[ CAS No. 3131-63-3 ] {[proInfo.proName]}

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2D 3D

Structure of 3131-63-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 3131-63-3 ]

COA NMR CNMR HPLC LC-MS

Related Doc. of [ 3131-63-3 ]

SDS Specification

Alternatived Products of [ 3131-63-3 ]

Product Details of [ 3131-63-3 ]

CAS No. :	3131-63-3	MDL No. :	MFCD00047287
Formula :	C₁₀H₁₀O	Boiling Point :	No data available
Linear Structure Formula :	-	InChI Key :	KJHYAEZMOHLVCH-UHFFFAOYSA-N
M.W :	146.19	Pubchem ID :	76582
Synonyms :

Safety of [ 3131-63-3 ]

Signal Word:	Warning	Class:
Precautionary Statements:	P261-P301+P312-P302+P352-P304+P340-P305+P351+P338	UN#:
Hazard Statements:	H302-H315-H319-H335	Packing Group:
GHS Pictogram:

Application In Synthesis of [ 3131-63-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

Upstream synthesis route of [ 3131-63-3 ]
Downstream synthetic route of [ 3131-63-3 ]

[ 3131-63-3 ] Synthesis Path-Upstream 1~1

1
[ 3131-63-3 ]
[ 3562-84-3 ]

Reference： [1] Journal of the Chemical Society, 1957, p. 625,627
[2] Journal of Medicinal Chemistry, 2011, vol. 54, # 8, p. 2701 - 2713
[3] Patent: WO2012/48058, 2012, A2,

[ 3131-63-3 ] Synthesis Path-Downstream 1~12

1
[ 113234-63-2 ]
[ 3131-63-3 ]
[ 4265-25-2 ]

Reference： [1]Tetrahedron Letters,1987,vol. 28,p. 3717 - 3718

2
[ 113234-63-2 ]
[ 3131-63-3 ]
[ 4265-25-2 ]
[ 791-28-6 ]

Reference： [1]Journal of the Chemical Society. Perkin transactions I,1994,p. 2455 - 2460

3
[ 113234-66-5 ]
[ 7522-79-4 ]
[ 3131-63-3 ]
[ 4265-25-2 ]

Reference： [1]Tetrahedron Letters,1987,vol. 28,p. 3717 - 3718

4
[ 113234-66-5 ]
[ 7522-79-4 ]
[ 3131-63-3 ]
[ 4265-25-2 ]
[ 791-28-6 ]

Reference： [1]Journal of the Chemical Society. Perkin transactions I,1994,p. 2455 - 2460

5
[ 113234-67-6 ]
[ 7522-79-4 ]
[ 3131-63-3 ]
[ 4265-25-2 ]

Reference： [1]Tetrahedron Letters,1987,vol. 28,p. 3717 - 3718

6
[ 113234-67-6 ]
[ 7522-79-4 ]
[ 3131-63-3 ]
[ 4265-25-2 ]
[ 791-28-6 ]

Reference： [1]Journal of the Chemical Society. Perkin transactions I,1994,p. 2455 - 2460

7
[ 113234-68-7 ]
[ 7522-79-4 ]
[ 3131-63-3 ]
[ 4265-25-2 ]

Reference： [1]Tetrahedron Letters,1987,vol. 28,p. 3717 - 3718

8
[ 113234-68-7 ]
[ 106-98-9 ]
[ 7522-79-4 ]
[ 3131-63-3 ]
[ 4265-25-2 ]
[ 791-28-6 ]

Reference： [1]Journal of the Chemical Society. Perkin transactions I,1994,p. 2455 - 2460

9
[ 513-86-0 ]
[ 5077-67-8 ]
[ 116-09-6 ]
[ 108-95-2 ]
[ 3131-63-3 ]
[ 3782-00-1 ]
[ 4265-25-2 ]

Yield	Reaction Conditions	Operation in experiment
	8percent Mo on gamma-alumina containing 1-2percent dispersed silica; at 145℃; for 2h;Conversion of starting material;	[0032] A feed containing 990 ppm hydroacetone (HA or acetol), 520 ppm of 1-hydroxy-2-butanone (1HB), and 490 ppm of 3-hydroxy-2-butanone (3HB or acetoin), was prepared from pure phenol and contacted for 2 hours at 145° C. with an alumina catalyst containing approximately 8 percent molybdenum. The catalyst was previously activated and dried. Conversion of hydroxyketones averaged 98, 98, and 100 percent for HA, 1HB, and 3HB, respectively, for three separate experiments. Approximately 6 percent of the HA was converted to 2-methyl benzofuran, 3 percent of the 1-HB was converted to 2-ethyl benzofuran, and 3 percent of 3-HB was converted to 1,3-dimethyl benzofuran.
	gamma-alumina Containing 1-2percent Dispersed Silica; at 145℃; for 2h;Conversion of starting material;	[0034] A feed containing 990 ppm HA, 520 ppm of 1HB, and 490 ppm of 3HB was prepared from pure phenol and contacted for 2 hours at 145° C. with an alumina catalyst containing no molybdenum and which had been previously activated and dried. Conversion of hydroxyketones were 18, 15, and 8 percent for HA, 1HB, and 3HB, respectively. The corresponding benzofuran selectivities were approximately 2, 0.5, and 2 percent.
	4percent Mo on gamma-alumina Containing 1-2percent Dispersed Silica; at 145℃; for 2h;Conversion of starting material;	[0033] A feed containing 990 ppm hydroacetone (HA or acetol), 520 ppm of 1-hydroxy-2-butanone (1HB), and 490 ppm 3-hydroxy-2-butanone (3HB or acetoin), was prepared from pure phenol and contacted for 2 hours at 145° C. with an alumina catalyst containing approximately 4 percent molybdenum. The catalyst was previously activated and dried. Conversion of hydroxyketones averaged 84, 87 and 98 percent for HA, 1HB, and 3HB, respectively, for three separate experiments. The corresponding benzofuran selectivities averaged approximately 6, 3, and 2.5 percent.

	at 145℃; for 2h;Conversion of starting material;	[0035] A feed containing 990 ppm HA, 520 ppm of 1HB and 490 ppm of 3HB was prepared from pure phenol and heated for 2 hours at 145° C. without addition of a catalyst. Conversion of hydroxyketones averaged 5, 5, and 7 percent for HA, 1HB, and 3HB, respectively, for three separate experiments. The corresponding benzofuran selectivities averaged approximately 3, 0.1, and 3 percent.
	at 145℃; for 2h;Conversion of starting material;	A feed containing 990 ppm hydroacetone (HA or acetol), 520 ppm of 1-hydroxy-2-butanone (1HB), and 490 ppm of 3- HYDROXY-2-BUTANONE (3HB or acetoin), was prepared from pure phenol and contacted for 2 hours at 145 C with an alumina catalyst containing approximately 8 percent molybdenum. The catalyst was previously activated and dried. Conversion of hydroxyketones averaged 98,98, and 100 percent for HA, 1HB, and 3HB, respectively, for three separate experiments. Approximately 6 percent of the HA was converted to 2-methyl benzofuran, 3 percent of the 1-HB was converted to 2-ethyl benzofuran, and 3 percent of 3-HB was converted to 1,3- dimethyl benzofuran.
	aluminum oxide; at 145℃; for 2h;Conversion of starting material;	A feed containing 990 ppm HA, 520 ppm of 1HB, and 490 ppm of 3HB was prepared from pure phenol and contacted for 2 hours at 145 C with an alumina catalyst containing no molybdenum and which had been previously activated and dried. Conversion of hydroxyketones were 18,15, and 8 percent for HA, 1HB, and 3HB, respectively. The corresponding benzofuran selectivities were approximately 2,0. 5, and 2 percent.
	at 145℃; for 2h;Conversion of starting material;	A feed containing 990 ppm hydroacetone (HA or acetol), 520 ppm of 1-hydroxy-2-butanone (1HB), and 490 ppm 3-hydroxy- 2-butanone (3HB or acetoin), was prepared from pure phenol and contacted for 2 hours at 145°C with an alumina catalyst containing approximately 4 percent molybdenum. The catalyst was previously activated and dried. Conversion of hydroxyketones averaged 84,87 and 98 percent for HA, 1HB, and 3HB, respectively, for three separate experiments. The corresponding benzofuran selectivities averaged approximately 6,3, and 2.5 percent.
	at 145℃; for 2h;Conversion of starting material;	A feed containing 990 ppm HA, 520 ppm of 1HB and 490 ppm of 3HB was prepared from pure phenol and heated for 2 hours at 145 C without addition of a catalyst. Conversion of hydroxyketones averaged 5,5, and 7 percent for HA, 1HB, and 3HB, respectively, for three separate experiments. The corresponding benzofuran selectivities averaged approximately 3,0. 1, and 3 percent.

Reference： [1]Patent: US2004/158106,2004,A1 .Location in patent: Page 3
[2]Patent: US2004/158106,2004,A1 .Location in patent: Page 3
[3]Patent: US2004/158106,2004,A1 .Location in patent: Page 3
[4]Patent: US2004/158106,2004,A1 .Location in patent: Page 3
[5]Patent: WO2004/72009,2004,A1 .Location in patent: Page 10
[6]Patent: WO2004/72009,2004,A1 .Location in patent: Page 11
[7]Patent: WO2004/72009,2004,A1 .Location in patent: Page 11
[8]Patent: WO2004/72009,2004,A1 .Location in patent: Page 11

10
[ 513-86-0 ]
[ 5077-67-8 ]
[ 116-09-6 ]
[ 3131-63-3 ]
[ 3782-00-1 ]
[ 4265-25-2 ]

Yield	Reaction Conditions	Operation in experiment
	amberlyst 15 (TM) cation exchange resin; at 80℃; for 2h;Conversion of starting material;	[0046] A feed containing 1450 ppm hydroxyacetone (HA or acetol), 520 ppm of 1-hydroxy-2-butanone (1HB), and 540 ppm of 3-hydroxy-2-butanone (3HB or acetoin) was prepared from pure phenol. The feed was stirred for 2 hours at 80° C. with Amberlyst 15 (TM) cation exchange resin beads which had previously been water rinsed and vacuum dried. Conversion of the hydroxyketones was 94 percent for HA, 74 percent for 1HB, and 80 percent for 3HB. Approximately 6 percent of the HA was converted to 2-MBF (2-methyl benzofuran), 3 percent of the 1HB was converted to EBF (2-ethyl benzofuran), and 24 percent of the 3HB was converted to DMBF (1,3 dimethyl benzofuran).
	Y-zeolite catalyst; at 150℃; for 2h;Conversion of starting material;	[0047] A feed containing 1000 ppm HA, 5300 ppm of 1HB, and 1050 ppm of 3HB was prepared from pure phenol and contacted for 2 hours at 150° C. with a Y-zeolite catalyst which had been previously activated and dried. The percent conversions of hydroxyketones were 93 for HA, 84 for 1HB, and 89 for 3HB. The corresponding benzofuran selectives were 33, 18 and 68 percent.
	alumina catalyst containing approximately 4 percent molybdenum; at 145℃; for 2h;Conversion of starting material;	[0049] A feed containing 990 ppm HA, 520 ppm of 1HB, and 490 ppm 3HB was prepared from pure phenol and contacted for 2 hours at 145° C. with an alumina catalyst containing approximately 4 percent molybdenum. The catalyst was previously activated and dried. Conversion of hydroxyketones were 84, 87 and 98 percent for HA, 1HB, and 3HB. The corresponding benzofuran selectivities averaged approximately 6, 3, and 2.5 percent.

	alumina catalyst containing approximately 8 percent molybdenum; at 145℃; for 2h;Conversion of starting material;	[0048] A feed containing 990 ppm HA, 520 ppm of 1HB, and 490 ppm of 3HB was prepared from pure phenol and contacted for 2 hours at 145° C. with an alumina catalyst containing approximately 8 percent molybdenum. The catalyst was previously activated and dried. Conversion of hydroxyketones averaged 98, 98, and 100 percent for HA, 1HB, and 3HB, respectively, for three separate experiments. The corresponding benzofuran selectivities averaged approximately 6, 3, and 3 percent
		[0050] A feed containing 990 ppm HA, 520 ppm of 1HB, and 490 ppm of 3HB was prepared from pure phenol and contacted for 2 hours at 145° C. with an alumina catalyst containing no molybdenum and which had been previously activated and dried. Conversion of hydroxyketones averaged 18, 15, and 8 percent for HA, 1HB, and 3HB, respectively, for three separate experiments. The corresponding benzofuran selectivities were approximately 2, 0.5, and 2 percent.
	Conversion of starting material;	[0051] A feed containing 990 ppm HA, 520 ppm of 1HB and 490 ppm of 3HB was prepared from pure phenol and heated for 2 hours at 145° C. without addition of a catalyst. Conversion of hydroxyketones averaged 5, 5, and 7 percent for HA, 1HB, and 3HB, respectively, for three separate experiments. The corresponding benzofuran selectivities averaged approximately 3, 0.1, and 3 percent.

Reference： [1]Patent: US2004/158105,2004,A1 .Location in patent: Page 5
[2]Patent: US2004/158105,2004,A1 .Location in patent: Page 5
[3]Patent: US2004/158105,2004,A1 .Location in patent: Page 5
[4]Patent: US2004/158105,2004,A1 .Location in patent: Page 5
[5]Patent: US2004/158105,2004,A1 .Location in patent: Page 5
[6]Patent: US2004/158105,2004,A1 .Location in patent: Page 5

11
[ 3131-63-3 ]
[ 88377-29-1 ]
2-ethyl-3-(2-bromo-3-methoxybenzoyl)benzofuran [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
47%		2-Bromo-3-methoxybenzoicacid (1a, 191 mg, 0.83 mmol) andSOCl2 (6.58 g, 55 mmol) were added to a round-bottom flask. Thereaction mixture was heated while refluxing for 2.0 hr and the solvent wasremoved under reduced pressure. The residue was diluted with CH2Cl2(8 mL) and SnCl4 (290 mg, 1.1 mmol), after which 2-ethylbenzofuran (120mg, 0.82 mmol) was added in an N2 atmosphere. The resulting mixturewas stirred for 2.5 hr at room temperature and cooled in an ice bath, followedby the addition of water (20 mL) to quench the reaction. The product wasextracted with CH2Cl2 and washed with brine. The organicphase was dried over anhydrous Na2SO4 and the solvent wasremoved under reduced pressure. The product was purified using silica gelcolumn chromatography. The yellow paste (140 mg, 47percent yield) was identified as 2-ethyl-3-(2-bromo-3-methoxybenzoyl)benzofuranon the basis of 1H-NMR and mass spectra. 1H-NMR (400 MHz,CDCl3): d1.17 (t, J=7.6 Hz, -CH2-CH3,3H), 2.67 (q, J=7.6 Hz, -CH2-CH3,2H), 3.93 (s, -OCH3, 3H), 7.08 (dd, J=7.4, 1.4 Hz, Ar H, 1H), 7.26-7.40 (m, Ar H, 4H), 7.54 (dd, J=8.2, 0.8 Hz, Ar H, 1H), 7.65 (d, J=8.2 Hz, Ar H, 1H); MS (ESI): m/z [M+Na+2]+ 383, [M+Na]+381.

Reference： [1]Bioorganic and Medicinal Chemistry Letters,2018,vol. 28,p. 3708 - 3711

12
[ 3131-63-3 ]
[ 88377-29-1 ]
2-ethyl-3-(2-bromo-3-hydroxybenzoyl)benzofuran [ No CAS ]

Reference： [1]Bioorganic and Medicinal Chemistry Letters,2018,vol. 28,p. 3708 - 3711

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Ghs Precautionary Statements

Precautionary Statements-General
Code	Phrase
P101	If medical advice is needed,have product container or label at hand.
P102	Keep out of reach of children.
P103	Read label before use
Prevention
Code	Phrase
P201	Obtain special instructions before use.
P202	Do not handle until all safety precautions have been read and understood.
P210	Keep away from heat/sparks/open flames/hot surfaces. - No smoking.
P211	Do not spray on an open flame or other ignition source.
P220	Keep/Store away from clothing/combustible materials.
P221	Take any precaution to avoid mixing with combustibles
P222	Do not allow contact with air.
P223	Keep away from any possible contact with water, because of violent reaction and possible flash fire.
P230	Keep wetted
P231	Handle under inert gas.
P232	Protect from moisture.
P233	Keep container tightly closed.
P234	Keep only in original container.
P235	Keep cool
P240	Ground/bond container and receiving equipment.
P241	Use explosion-proof electrical/ventilating/lighting/equipment.
P242	Use only non-sparking tools.
P243	Take precautionary measures against static discharge.
P244	Keep reduction valves free from grease and oil.
P250	Do not subject to grinding/shock/friction.
P251	Pressurized container: Do not pierce or burn, even after use.
P260	Do not breathe dust/fume/gas/mist/vapours/spray.
P261	Avoid breathing dust/fume/gas/mist/vapours/spray.
P262	Do not get in eyes, on skin, or on clothing.
P263	Avoid contact during pregnancy/while nursing.
P264	Wash hands thoroughly after handling.
P265	Wash skin thouroughly after handling.
P270	Do not eat, drink or smoke when using this product.
P271	Use only outdoors or in a well-ventilated area.
P272	Contaminated work clothing should not be allowed out of the workplace.
P273	Avoid release to the environment.
P280	Wear protective gloves/protective clothing/eye protection/face protection.
P281	Use personal protective equipment as required.
P282	Wear cold insulating gloves/face shield/eye protection.
P283	Wear fire/flame resistant/retardant clothing.
P284	Wear respiratory protection.
P285	In case of inadequate ventilation wear respiratory protection.
P231 + P232	Handle under inert gas. Protect from moisture.
P235 + P410	Keep cool. Protect from sunlight.
Response
Code	Phrase
P301	IF SWALLOWED:
P304	IF INHALED:
P305	IF IN EYES:
P306	IF ON CLOTHING:
P307	IF exposed:
P308	IF exposed or concerned:
P309	IF exposed or if you feel unwell:
P310	Immediately call a POISON CENTER or doctor/physician.
P311	Call a POISON CENTER or doctor/physician.
P312	Call a POISON CENTER or doctor/physician if you feel unwell.
P313	Get medical advice/attention.
P314	Get medical advice/attention if you feel unwell.
P315	Get immediate medical advice/attention.
P320
P302 + P352	IF ON SKIN: wash with plenty of soap and water.
P321
P322
P330	Rinse mouth.
P331	Do NOT induce vomiting.
P332	IF SKIN irritation occurs:
P333	If skin irritation or rash occurs:
P334	Immerse in cool water/wrap n wet bandages.
P335	Brush off loose particles from skin.
P336	Thaw frosted parts with lukewarm water. Do not rub affected area.
P337	If eye irritation persists:
P338	Remove contact lenses, if present and easy to do. Continue rinsing.
P340	Remove victim to fresh air and keep at rest in a position comfortable for breathing.
P341	If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P342	If experiencing respiratory symptoms:
P350	Gently wash with plenty of soap and water.
P351	Rinse cautiously with water for several minutes.
P352	Wash with plenty of soap and water.
P353	Rinse skin with water/shower.
P360	Rinse immediately contaminated clothing and skin with plenty of water before removing clothes.
P361	Remove/Take off immediately all contaminated clothing.
P362	Take off contaminated clothing and wash before reuse.
P363	Wash contaminated clothing before reuse.
P370	In case of fire:
P371	In case of major fire and large quantities:
P372	Explosion risk in case of fire.
P373	DO NOT fight fire when fire reaches explosives.
P374	Fight fire with normal precautions from a reasonable distance.
P376	Stop leak if safe to do so. Oxidising gases (section 2.4) 1
P377	Leaking gas fire: Do not extinguish, unless leak can be stopped safely.
P378
P380	Evacuate area.
P381	Eliminate all ignition sources if safe to do so.
P390	Absorb spillage to prevent material damage.
P391	Collect spillage. Hazardous to the aquatic environment
P301 + P310	IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P301 + P312	IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P301 + P330 + P331	IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P302 + P334	IF ON SKIN: Immerse in cool water/wrap in wet bandages.
P302 + P350	IF ON SKIN: Gently wash with plenty of soap and water.
P303 + P361 + P353	IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P304 + P312	IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell.
P304 + P340	IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P304 + P341	IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P305 + P351 + P338	IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P306 + P360	IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes.
P307 + P311	IF exposed: call a POISON CENTER or doctor/physician.
P308 + P313	IF exposed or concerned: Get medical advice/attention.
P309 + P311	IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician.
P332 + P313	IF SKIN irritation occurs: Get medical advice/attention.
P333 + P313	IF SKIN irritation or rash occurs: Get medical advice/attention.
P335 + P334	Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages.
P337 + P313	IF eye irritation persists: Get medical advice/attention.
P342 + P311	IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician.
P370 + P376	In case of fire: Stop leak if safe to Do so.
P370 + P378	In case of fire:
P370 + P380	In case of fire: Evacuate area.
P370 + P380 + P375	In case of fire: Evacuate area. Fight fire remotely due to the risk of explosion.
P371 + P380 + P375	In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion.
Storage
Code	Phrase
P401
P402	Store in a dry place.
P403	Store in a well-ventilated place.
P404	Store in a closed container.
P405	Store locked up.
P406	Store in corrosive resistant/ container with a resistant inner liner.
P407	Maintain air gap between stacks/pallets.
P410	Protect from sunlight.
P411
P412	Do not expose to temperatures exceeding 50 oC/ 122 oF.
P413
P420	Store away from other materials.
P422
P402 + P404	Store in a dry place. Store in a closed container.
P403 + P233	Store in a well-ventilated place. Keep container tightly closed.
P403 + P235	Store in a well-ventilated place. Keep cool.
P410 + P403	Protect from sunlight. Store in a well-ventilated place.
P410 + P412	Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF.
P411 + P235	Keep cool.
Disposal
Code	Phrase
P501	Dispose of contents/container to ...
P502	Refer to manufacturer/supplier for information on recovery/recycling

Physical hazards
Code	Phrase
H200	Unstable explosive
H201	Explosive; mass explosion hazard
H202	Explosive; severe projection hazard
H203	Explosive; fire, blast or projection hazard
H204	Fire or projection hazard
H205	May mass explode in fire
H220	Extremely flammable gas
H221	Flammable gas
H222	Extremely flammable aerosol
H223	Flammable aerosol
H224	Extremely flammable liquid and vapour
H225	Highly flammable liquid and vapour
H226	Flammable liquid and vapour
H227	Combustible liquid
H228	Flammable solid
H229	Pressurized container: may burst if heated
H230	May react explosively even in the absence of air
H231	May react explosively even in the absence of air at elevated pressure and/or temperature
H240	Heating may cause an explosion
H241	Heating may cause a fire or explosion
H242	Heating may cause a fire
H250	Catches fire spontaneously if exposed to air
H251	Self-heating; may catch fire
H252	Self-heating in large quantities; may catch fire
H260	In contact with water releases flammable gases which may ignite spontaneously
H261	In contact with water releases flammable gas
H270	May cause or intensify fire; oxidizer
H271	May cause fire or explosion; strong oxidizer
H272	May intensify fire; oxidizer
H280	Contains gas under pressure; may explode if heated
H281	Contains refrigerated gas; may cause cryogenic burns or injury
H290	May be corrosive to metals
Health hazards
Code	Phrase
H300	Fatal if swallowed
H301	Toxic if swallowed
H302	Harmful if swallowed
H303	May be harmful if swallowed
H304	May be fatal if swallowed and enters airways
H305	May be harmful if swallowed and enters airways
H310	Fatal in contact with skin
H311	Toxic in contact with skin
H312	Harmful in contact with skin
H313	May be harmful in contact with skin
H314	Causes severe skin burns and eye damage
H315	Causes skin irritation
H316	Causes mild skin irritation
H317	May cause an allergic skin reaction
H318	Causes serious eye damage
H319	Causes serious eye irritation
H320	Causes eye irritation
H330	Fatal if inhaled
H331	Toxic if inhaled
H332	Harmful if inhaled
H333	May be harmful if inhaled
H334	May cause allergy or asthma symptoms or breathing difficulties if inhaled
H335	May cause respiratory irritation
H336	May cause drowsiness or dizziness
H340	May cause genetic defects
H341	Suspected of causing genetic defects
H350	May cause cancer
H351	Suspected of causing cancer
H360	May damage fertility or the unborn child
H361	Suspected of damaging fertility or the unborn child
H361d	Suspected of damaging the unborn child
H362	May cause harm to breast-fed children
H370	Causes damage to organs
H371	May cause damage to organs
H372	Causes damage to organs through prolonged or repeated exposure
H373	May cause damage to organs through prolonged or repeated exposure
Environmental hazards
Code	Phrase
H400	Very toxic to aquatic life
H401	Toxic to aquatic life
H402	Harmful to aquatic life
H410	Very toxic to aquatic life with long-lasting effects
H411	Toxic to aquatic life with long-lasting effects
H412	Harmful to aquatic life with long-lasting effects
H413	May cause long-lasting harmful effects to aquatic life
H420	Harms public health and the environment by destroying ozone in the upper atmosphere

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[ CAS No. 3131-63-3 ] {[proInfo.proName]}

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[ 3131-63-3 ] Synthesis Path-Upstream 1~1

[ 3131-63-3 ] Synthesis Path-Downstream 1~12

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Benzofurans

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