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[ CAS No. 31786-45-5 ] {[proInfo.proName]}

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Chemical Structure| 31786-45-5
Chemical Structure| 31786-45-5
Structure of 31786-45-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 31786-45-5 ]

CAS No. :31786-45-5 MDL No. :MFCD00800732
Formula : C8H7BrO3 Boiling Point : -
Linear Structure Formula :- InChI Key :BNYFDICJYCBPRW-UHFFFAOYSA-N
M.W : 231.04 Pubchem ID :11117881
Synonyms :

Calculated chemistry of [ 31786-45-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.59
TPSA : 46.53 ?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) : -6.73 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.5
Log Po/w (XLOGP3) : 1.38
Log Po/w (WLOGP) : 2.16
Log Po/w (MLOGP) : 2.06
Log Po/w (SILICOS-IT) : 1.89
Consensus Log Po/w : 1.8

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.38
Solubility : 0.963 mg/ml ; 0.00417 mol/l
Class : Soluble
Log S (Ali) : -1.96
Solubility : 2.53 mg/ml ; 0.011 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.76
Solubility : 0.403 mg/ml ; 0.00175 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.52

Safety of [ 31786-45-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 31786-45-5 ]

* 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 [ 31786-45-5 ]

[ 31786-45-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 6494-19-5 ]
  • [ 31786-45-5 ]
  • [ 126955-75-7 ]
YieldReaction ConditionsOperation in experiment
7.45 g (75.9%) With hydrogenchloride; potassium carbonate; In water; nitrobenzene; Step A 3-Methyl-6-nitroindazole (5.31 g), 6.93 g of 2-bromo-6-methoxybenzoic acid, 4.71 g of potassium carbonate and 0.218 g of copper (II) oxide were stirred in 60 ml of nitrobenzene at 180° C. for 50 minutes. After cooling, 300 ml of water was added to the reaction mixture, and the insoluble substance was removed by filtration. The resulting solution was washed with chloroform. The aqueous layer was decolored with active charcoal and filtered, and 40 ml of 1 N hydrochloric acid aqueous solution was added to the filtrate. The crystals precipitated were separated by filtration and dried under reduced pressure to obtain 7.45 g (75.9percent) of 1-(2-carboxy-3-methoxyphenyl)-<strong>[6494-19-5]3-methyl-6-nitroindazole</strong>.
  • 2
  • [ 126712-07-0 ]
  • [ 31786-45-5 ]
  • 3
  • [ 124-38-9 ]
  • [ 95970-22-2 ]
  • [ 31786-45-5 ]
  • [ 88377-29-1 ]
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