METHYL 2-BROMO-3-NITROBENZOATE

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Products Intro: Product Name:Methyl 2-bromo-3-nitrobenzoate
CAS:5337-09-7
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:5337-09-7
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CAS:5337-09-7
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CAS: 5337-09-7
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CAS:5337-09-7
Purity:0.97 Package:1KG;25KG

METHYL 2-BROMO-3-NITROBENZOATE manufacturers

METHYL 2-BROMO-3-NITROBENZOATE Basic information
Product Name:METHYL 2-BROMO-3-NITROBENZOATE
Synonyms:3-Nitro-2-bromobenzoic acid methyl ester;METHYL 2-BROMO-3-NITROBENZOATE;2-BROMO-3-NITRO-BENZOIC ACID METHYL ESTER;2-bromo-3-nitro-benzoicacimethylester;Benzoic acid, 2-bromo-3-nitro-, methyl ester
CAS:5337-09-7
MF:C8H6BrNO4
MW:260.04
EINECS:
Product Categories:pharmacetical
Mol File:5337-09-7.mol
METHYL 2-BROMO-3-NITROBENZOATE Structure
METHYL 2-BROMO-3-NITROBENZOATE Chemical Properties
Melting point 77 °C(Solv: methanol (67-56-1))
Boiling point 300.0±20.0 °C(Predicted)
density 1.673±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform, DCM, Ethyl Acetate
form Solid
color Off-White
EPA Substance Registry SystemBenzoic acid, 2-bromo-3-nitro-, methyl ester (5337-09-7)
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
HS Code 2916310090
MSDS Information
METHYL 2-BROMO-3-NITROBENZOATE Usage And Synthesis
Uses2-Bromo-3-nitrobenzoic Acid Methyl Ester is an halogenated benzoic acid and an intermediate in the synthesis of anti-inflammatory drug Balsalazide (B116300).
Synthesis
Methanol

67-56-1

2-Bromo-3-nitrobenzoic acid

573-54-6

METHYL 2-BROMO-3-NITROBENZOATE

5337-09-7

General procedure for the synthesis of methyl 2-bromo-3-nitrobenzoate from methanol and 2-bromo-3-nitrobenzoic acid: Example 4: 100 g (406 mmol) of 2-bromo-3-nitrobenzoic acid and 22 g (609 mmol) of concentrated hydrochloric acid were added to a reactor followed by 1 liter of methanol. The reaction mixture was heated under reflux conditions for 24 hours. After completion of the reaction, it was cooled to room temperature and the precipitated solid product was collected by filtration. The solid was washed sequentially with deionized water and ethanol and then dried. Finally, the dried product was purified by recrystallization with ethanol. Methyl 2-bromo-3-nitrobenzoate 94.6 g (363 mmol) was obtained in 89.5% yield of the theoretical value.

References[1] Patent: US2015/148550, 2015, A1. Location in patent: Paragraph 0167; 0168; 0169; 0170; 0171; 0172
[2] Tetrahedron, 2000, vol. 56, # 2, p. 165 - 173
[3] Patent: US9337430, 2016, B2. Location in patent: Page/Page column 117
[4] Bioorganic and Medicinal Chemistry Letters, 1997, vol. 7, # 11, p. 1399 - 1402
[5] Molecular Pharmacology, 2013, vol. 84, # 5, p. 726 - 735
Tag:METHYL 2-BROMO-3-NITROBENZOATE(5337-09-7) Related Product Information
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