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[ CAS No. 923266-17-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 923266-17-5
Chemical Structure| 923266-17-5
Structure of 923266-17-5 * Storage: {[proInfo.prStorage]}
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Product Details of [ 923266-17-5 ]

CAS No. :923266-17-5 MDL No. :MFCD10000928
Formula : C9H6BrFO2 Boiling Point : -
Linear Structure Formula :- InChI Key :LHHBEQSDZPKXEI-DUXPYHPUSA-N
M.W : 245.05 Pubchem ID :67456639
Synonyms :

Calculated chemistry of [ 923266-17-5 ]

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 50.77
TPSA : 37.3 Ų

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) : -5.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.94
Log Po/w (XLOGP3) : 2.65
Log Po/w (WLOGP) : 3.0
Log Po/w (MLOGP) : 3.03
Log Po/w (SILICOS-IT) : 2.81
Consensus Log Po/w : 2.69

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.85

Water Solubility

Log S (ESOL) : -3.24
Solubility : 0.142 mg/ml ; 0.000578 mol/l
Class : Soluble
Log S (Ali) : -3.08
Solubility : 0.202 mg/ml ; 0.000823 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.0
Solubility : 0.246 mg/ml ; 0.001 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.96

Safety of [ 923266-17-5 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501 UN#:
Hazard Statements:H302-H312-H332 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 923266-17-5 ]

* 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 [ 923266-17-5 ]

[ 923266-17-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 923266-17-5 ]
  • [ 541-41-3 ]
  • C12H10BrFO4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine In acetone at 0 - 5℃; for 1h; c To a solution of 4.0 g (16.3 mmol) of 3-(4-bromo-3-fluoro-phenyl)-acrylic acid in 60 mL acetone were subsequently added at 0 - 5°C 2.0 g (19.6 mmol) triethylamine in 10 mL of acetone followed by 2.3 g (21.2 mmol) of ethyl chloroformate in 10 mL of acetone. After stirring for 1 h at 0 - 5°C a solution of 1.6 g (24.5 mmol) of sodium azide in 9 mL of water was added. After stirring for 1 additional h the reaction mixture was poured onto 200 mL ice water and extraced with chloroform twice. The organic phase was dried over magnesium sulfate, 24 mL of diphenylether were added and the chloroform was cautiously removed in vacuo. The residue was then added dropwise into 60 mL of diphenylether, which had been preheated to 2500C. After complete addition the reaction mixture was stirred for additional 30 minutes at 230 - 2500C. After cooling EPO down to 1000C the reaction mixture was poured into 100 ml_ of heptane and after further cooling in an ice bath the precipitated product was filtered by suction and 2.4 g of crude 7-bromo-6-fluoro-2H-isoquinolin-1-one were obtained.
  • 2
  • [ 923266-16-4 ]
  • [ 923266-17-5 ]
YieldReaction ConditionsOperation in experiment
Stage #1: 3-(4-bromo-3-fluoro-phenyl)-acrylic acid ethyl ester With sodium hydroxide; water In methanol Stage #2: With hydrogenchloride In methanol; water b 10.5 g (38.6 mmol) of 3-(4-bromo-3-fluoro-phenyl)-acrylic acid ethyl ester were dissolved in 100 mL of methanol and stirred overnight with 97 mL of aqueous 1 M sodium hydroxide solution. After removal of the methanol in vacuo the residue was acidified with concentrated hydrochloric acid. The precipitate was isolated by suction and dried in vacuo at 500C furnishing 8.0 g of 3-(4-bromo-3-fluoro-phenyl)-acrylic acid.
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