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5-BROMO-2-METHYL-3-NITROBENZOIC ACID

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Products Intro: Product Name:5-Bromo-2-methyl-3-nitrobenzoic acid
CAS:107650-20-4
Purity:99% Package:1KG;5USD|1000KG;0.5USD
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Products Intro: Product Name:5-Bromo-2-methyl-3-nitrobenzoic acid
CAS:107650-20-4
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:107650-20-4
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Products Intro: Product Name:5-BROMO-2-METHYL-3-NITROBENZOIC ACID
CAS:107650-20-4
Purity:0.98 Package:1kg;5kg;25kg
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Products Intro: Product Name:5-Bromo-2-methyl-3-nitrobenzoic acid
CAS:107650-20-4
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-23419

5-BROMO-2-METHYL-3-NITROBENZOIC ACID manufacturers

5-BROMO-2-METHYL-3-NITROBENZOIC ACID Basic information
Product Name:5-BROMO-2-METHYL-3-NITROBENZOIC ACID
Synonyms:Benzoic acid, 5-broMo-2-Methyl-3-nitro-;AKOS BB-9545;5-BROMO-2-METHYL-3-NITROBENZOIC ACID;-3-nitrobenzoic acid;5-Bromo-2-methyl-3-nitrobenzoicAci;5-BROMO-2-METHYL-3-NITROBENZOIC ACID ISO 9001:2015 REACH
CAS:107650-20-4
MF:C8H6BrNO4
MW:260.04
EINECS:
Product Categories:
Mol File:107650-20-4.mol
5-BROMO-2-METHYL-3-NITROBENZOIC ACID Structure
5-BROMO-2-METHYL-3-NITROBENZOIC ACID Chemical Properties
Boiling point 377.0±42.0 °C(Predicted)
density 1.777±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka2+-.0.20(Predicted)
InChIInChI=1S/C8H6BrNO4/c1-4-6(8(11)12)2-5(9)3-7(4)10(13)14/h2-3H,1H3,(H,11,12)
InChIKeyDXUUJILVHXQDCV-UHFFFAOYSA-N
SMILESC1(C(C)=C(C(=O)O)C=C(Br)C=1)[N+]([O-])=O
Safety Information
MSDS Information
5-BROMO-2-METHYL-3-NITROBENZOIC ACID Usage And Synthesis
Uses5-Bromo-2-methyl-3-nitrobenzoic Acid is a reactant in the preparation of EPZ005687 (E592200), a potent and selective inhibitor of EZH2.
Synthesis
2-Methyl-3-nitrobenzoic acid

1975-50-4

5-BROMO-2-METHYL-3-NITROBENZOIC ACID

107650-20-4

General procedure for the synthesis of 2-methyl-3-nitro-5-bromobenzoic acid from 2-methyl-3-nitrobenzoic acid: N-bromosuccinimide (15 g, 84.3 mmol) was added to a concentrated sulfuric acid solution (60 mL) containing 2-methyl-3-nitrobenzoic acid (15 g, 82.8 mmol). The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the reaction solution was slowly poured into ice water (400 mL). The precipitate was collected by filtration and dried under vacuum to give 21 g of the target product 2-methyl-3-nitro-5-bromobenzoic acid in 98% yield.

References[1] Patent: US2012/264734, 2012, A1. Location in patent: Page/Page column 100
[2] Patent: WO2012/142513, 2012, A1. Location in patent: Page/Page column 288
[3] Patent: US2014/107122, 2014, A1. Location in patent: Paragraph 0157; 0158
[4] Patent: WO2003/99275, 2003, A1. Location in patent: Page 101
[5] Patent: US2007/219212, 2007, A1. Location in patent: Page/Page column 23
Tag:5-BROMO-2-METHYL-3-NITROBENZOIC ACID(107650-20-4) Related Product Information
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