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[ CAS No. 6307-83-1 ] {[proInfo.proName]}

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Chemical Structure| 6307-83-1
Chemical Structure| 6307-83-1
Structure of 6307-83-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 6307-83-1 ]

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Product Details of [ 6307-83-1 ]

CAS No. :6307-83-1 MDL No. :MFCD00100098
Formula : C7H4BrNO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :AXRKIZCFYZBBPX-UHFFFAOYSA-N
M.W : 246.02 Pubchem ID :239336
Synonyms :

Calculated chemistry of [ 6307-83-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 49.92
TPSA : 83.12 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.09 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.06
Log Po/w (XLOGP3) : 2.41
Log Po/w (WLOGP) : 2.06
Log Po/w (MLOGP) : 1.27
Log Po/w (SILICOS-IT) : -0.22
Consensus Log Po/w : 1.31

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.09
Solubility : 0.199 mg/ml ; 0.000807 mol/l
Class : Soluble
Log S (Ali) : -3.8
Solubility : 0.0392 mg/ml ; 0.000159 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.01
Solubility : 2.4 mg/ml ; 0.00977 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.04

Safety of [ 6307-83-1 ]

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 [ 6307-83-1 ]

* 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 [ 6307-83-1 ]

[ 6307-83-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6307-83-1 ]
  • [ 42237-85-4 ]
YieldReaction ConditionsOperation in experiment
94% Concentrated hydrochloric acid (30 ml) was gradually added to a solution of the title compound of Preparation 49 (7.02 g, 28.54 mmols) and ethanol (150 ml), the solution was stirred at room temperature during five minutes. Then Tin (II) chloride was added and the solution was stirred at 50C for two hours. The solution was cooled at room temperature. The solution basified to pH 9 with 8M sodium hydroxide precipitating a solid. The solid was collected by filtration and discarded. The filtrate was acidified with hydrochloric acid to pH 5 and precipitation from this solution gave 5.8 g (94%) of the title compound. HPLC/MS (10 min) retention time 4.67 min LRMS: m/z 216 (M-1)
94% PREPARATION 21; 3-Amino-5-bromobenzoic acid [Show Image] Concentrated hydrochloric acid (30 mL) was gradually added to a solution of the title compound of Preparation 20 (7.02 g, 28.54 mmols) and ethanol (150 mL), the solution was stirred at room temperature during five minutes. Then Tin (II) chloride was added and the solution was stirred at 50C for two hours. The solution was cooled at room temperature. The solution basified to pH 9 with 8M sodium hydroxide precipitating a solid. The solid was collected by filtration and discarded. The filtrate was acidified with hydrochloric acid to pH 5 and precipitation from this solution gave 5.8 g (94%) of the title compound. HPLC/MS (10 min) retention time 4.67 min LRMS: m/z 216 (M-1)
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