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[ CAS No. 2343-89-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
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Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 2343-89-7
Chemical Structure| 2343-89-7
Structure of 2343-89-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2343-89-7 ]

CAS No. :2343-89-7 MDL No. :MFCD04039286
Formula : C4H5FO2 Boiling Point : -
Linear Structure Formula :- InChI Key :ZTZJVAOTIOAZGZ-UHFFFAOYSA-N
M.W : 104.08 Pubchem ID :2782524
Synonyms :

Calculated chemistry of [ 2343-89-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.25
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 22.2
TPSA : 26.3 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.21 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.67
Log Po/w (XLOGP3) : 1.02
Log Po/w (WLOGP) : 1.06
Log Po/w (MLOGP) : 0.59
Log Po/w (SILICOS-IT) : 0.56
Consensus Log Po/w : 0.98

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.0
Solubility : 10.5 mg/ml ; 0.101 mol/l
Class : Very soluble
Log S (Ali) : -1.16
Solubility : 7.17 mg/ml ; 0.0689 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.61
Solubility : 25.5 mg/ml ; 0.245 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.22

Safety of [ 2343-89-7 ]

Signal Word:Danger Class:3,6.1
Precautionary Statements:P273-P260-P210-P370+P378-P391-P301+P310+P330 UN#:1992
Hazard Statements:H301-H372-H411-H225 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2343-89-7 ]

* 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.

  • Downstream synthetic route of [ 2343-89-7 ]

[ 2343-89-7 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 2343-89-7 ]
  • [ 430-99-9 ]
  • 2
  • [ 67-56-1 ]
  • [ 420-25-7 ]
  • [ 201230-82-2 ]
  • [ 430-99-9 ]
  • [ 2343-89-7 ]
YieldReaction ConditionsOperation in experiment
14.1%; 70.9% With dichloro[bis(2-(diphenylphosphino)phenyl)ether]palladium(ll); triethylamine; at 100℃; under 7500.75 Torr; for 13h;Autoclave; 8.98 g (71.87 mmol) of 1-bromo-1-fluoroethene, 8.01 g (79.2 mmol) of triethylamine, 51.5 mg (0.072 mmol) of dichloro[bis(diphenylphosphinophenyl)ether]palladium (II), and 36 mE of non-dried methanol were placed in a 1 50-mE stainless autoclave, and 1.0 MPaG carbon monoxide was introduced thereto, followed by stirring at 100° C. for 13 hours. After completion of the reaction, the autoclave was cooled, and the unreacted gas was purged. The autoclave was opened, and 186 mg (1.0 mmol) of hexafluorobenzenewas added as an internal standard substance, followed by stirring. The mixture was then allowed to stand for a short period of time to precipitate the salt. The supernatant was diluted with deuterated chloroform, and subjected to quantification based on 19F-NMR integral values. The diluted supernatant was found to contain 50.93 mmol (yield: 70.9percent) of 2-fluoroacrylic acid methyl ester, 10.13 mmol (yield:14.1percent) of 2-fluoroacrylic acid, and 8.12 mmol (recovery:11.3percent) of unreacted 1 -bromo-1 -fluoroethene. The conversion was 87.5percent, and the selectivity was 81.0percent.
  • 3
  • [ 67-56-1 ]
  • [ 430-99-9 ]
  • [ 2343-89-7 ]
YieldReaction ConditionsOperation in experiment
93% With thionyl chloride; at 5 - 35℃; for 2h; 8.64 g (0.096 mol) of <strong>[430-99-9]2-fluoroacrylic acid</strong> was mixed in a 100 ml three-necked flask at 5-10 ° C,And 13.1 g (0.11 mol) of thionyl chloride were added, the temperature was raised to 30 ° C, 6.4 g (0.2 mol) of methanol was added dropwise,Insulation 30-35 reaction 2h,The system was neutralized by adding aqueous NaHCO3 solution,20 g (0.23 mol) of methyl t-butyl ether was added for extraction,The organic phase was distilled to give methyl 2-fluoroacrylate. Yield 93percent.
  • 4
  • [ 2343-89-7 ]
  • [ 50-43-1 ]
  • (Z)-methyl 2-fluoro-3-(2,4,6-trichlorophenyl)acrylate [ No CAS ]
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