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[ CAS No. 50739-76-9 ] {[proInfo.proName]}

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Chemical Structure| 50739-76-9
Chemical Structure| 50739-76-9
Structure of 50739-76-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 50739-76-9 ]

CAS No. :50739-76-9 MDL No. :MFCD06202693
Formula : C7H7Br2NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :GHUMSGGCKVMYGH-UHFFFAOYSA-N
M.W : 280.95 Pubchem ID :21320495
Synonyms :

Calculated chemistry of [ 50739-76-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 2.0
Molar Refractivity : 52.37
TPSA : 46.25 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.32 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.11
Log Po/w (XLOGP3) : 2.39
Log Po/w (WLOGP) : 2.14
Log Po/w (MLOGP) : 2.37
Log Po/w (SILICOS-IT) : 2.31
Consensus Log Po/w : 2.27

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.43
Solubility : 0.106 mg/ml ; 0.000376 mol/l
Class : Soluble
Log S (Ali) : -3.0
Solubility : 0.279 mg/ml ; 0.000994 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.57
Solubility : 0.0758 mg/ml ; 0.00027 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.34

Safety of [ 50739-76-9 ]

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

Application In Synthesis of [ 50739-76-9 ]

* 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 [ 50739-76-9 ]

[ 50739-76-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 606-00-8 ]
  • [ 50739-76-9 ]
YieldReaction ConditionsOperation in experiment
95% With potassium borohydride; ethanol; at 20 - 40℃; for 0.5h;Industrial scale; 10.0 kg of absolute ethanol and 5.88 kg of methyl 3,5-dibromo-2-aminobenzoate were added to a 100 L double-layer glass reactor.After stirring uniformly, 2.62 kg of potassium borohydride was added, and stirring was continued for 30 minutes at room temperature.The temperature of the reaction mixture was raised to 40 C, and 13.5 g of an anhydrous ethanol solution containing 2.7 kg of calcium chloride was slowly added to the reaction liquid for a period of not less than 6 hours.After the addition, the reaction was stirred for 8 hours, and the UPLC test was taken. After the reaction was passed (the methyl 3,5-dibromo-2-aminobenzoate was not more than 1.0%), and cooled to room temperature.The temperature of the reaction solution was maintained at not more than 35 C, and 32 kg of 5% hydrochloric acid was slowly added to the reaction solution to adjust the pH to 2 to 3, and stirring was continued for 20 minutes, and the pH was measured again.Centrifugally filter, rinse the filter cake with purified water to neutrality, and transfer the obtained solid to the reaction kettle.20 kg of a 0.4% sodium hydroxide solution was added, and the mixture was heated to 45 C and stirred for 15 minutes, and then cooled to room temperature.Centrifugal filtration, rinse the filter cake with purified water to neutrality. It is placed in a blast drying oven tray, dried at 60 C for 20 hours, and after receiving water, it is charged with 5.08 kg, and the yield is 95%.
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