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[ CAS No. 3674-13-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
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+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 3674-13-3
Chemical Structure| 3674-13-3
Structure of 3674-13-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 3674-13-3 ]

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Product Citations

Product Details of [ 3674-13-3 ]

CAS No. :3674-13-3 MDL No. :MFCD00000212
Formula : C5H8Br2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :OENICUBCLXKLJQ-UHFFFAOYSA-N
M.W : 259.92 Pubchem ID :97945
Synonyms :

Calculated chemistry of [ 3674-13-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.8
Num. rotatable bonds : 4
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 43.17
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) : -6.42 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.2
Log Po/w (XLOGP3) : 2.07
Log Po/w (WLOGP) : 1.71
Log Po/w (MLOGP) : 1.96
Log Po/w (SILICOS-IT) : 1.85
Consensus Log Po/w : 1.96

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.49
Solubility : 0.838 mg/ml ; 0.00322 mol/l
Class : Soluble
Log S (Ali) : -2.25
Solubility : 1.46 mg/ml ; 0.0056 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.52
Solubility : 0.781 mg/ml ; 0.00301 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.68

Safety of [ 3674-13-3 ]

Signal Word:Danger Class:8,6.1
Precautionary Statements:P501-P270-P210-P264-P280-P370+P378-P303+P361+P353-P301+P330+P331-P362-P301+P310+P330-P304+P340+P310-P305+P351+P338+P310-P403+P235-P405 UN#:2922
Hazard Statements:H301+H311-H314-H227 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 3674-13-3 ]

* 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.

  • Downstream synthetic route of [ 3674-13-3 ]

[ 3674-13-3 ] Synthesis Path-Downstream   1~6

  • 2
  • [ 38183-03-8 ]
  • [ 3674-13-3 ]
  • [ 121869-37-2 ]
  • [ 121869-36-1 ]
  • 3
  • [ 38183-03-8 ]
  • [ 3674-13-3 ]
  • 1360 [ No CAS ]
  • [ 121869-37-2 ]
  • [ 121869-36-1 ]
  • 4
  • [ 67247-13-6 ]
  • [ 3674-13-3 ]
  • ethyl 8-methoxy-2,3-dihydronaphtho[1,2-b]furan-2-carboxylate [ No CAS ]
  • ethyl 6'-methoxy-4'-oxospiro[cyclopropane-1,1'(4'H)-naphthalene]-2-carboxylate [ No CAS ]
  • 5
  • [ 3846-73-9 ]
  • [ 3674-13-3 ]
  • 8-methyl-2<i>H</i>-4-oxa-9b-aza-cyclopenta[<i>cd</i>]phenalene-1,2a-dicarboxylic acid diethyl ester [ No CAS ]
  • 6
  • [ 16713-45-4 ]
  • [ 3674-13-3 ]
  • [ 55876-82-9 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In 1,4-dioxane; EXAMPLE 6 Preparation of ethyl 5-methylpyridine-2-carboxylate 6.1 g of triethylamine are added at 0 C. to 13 g of ethyl 2,3-di-bromopropionate in 50 ml of dioxane. The mixture is stirred for 2 hours at room temperature and then a solution of 5.6 g of 1-dimethylamino-1-aza-3-methyl-1,3-butadiene and 6.1 g of triethylamine in 50 ml of dioxane is added dropwise. The reaction mixture is kept for 30 hours at 70 C. and then cooled and concentrated by evaporation. The residue is partitioned between water and ether and the organic phase is washed with brine, dried and concentrated by evaporation. The residue is distilled under reduced pressure, affording 3.2 g of the title compound as an oil with a boiling point of 69-74 C. (at 0.08 mbar).
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