5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER

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CAS:57800-76-7
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CAS:57800-76-7
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Products Intro: Product Name:5-Chloro-4-nitrothiophene-2-carboxylic acid methyl ester
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Products Intro: Product Name:5-Chloro-4-nitrothiophene-2-carboxylic acid methyl ester
CAS:57800-76-7
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5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER manufacturers

5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER Basic information
Product Name:5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER
Synonyms:5-Chlor-4-nitro-2-thiophencarbonsaeureMethylester;5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER;AKOS 91745;Methyl 5-chloro-4-nitro-2-thiophenecarboxylate;5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER, 95+%;2-Thiophenecarboxylic acid, 5-chloro-4-nitro-, methyl ester;Methyl 5-chloro-4-nitrothiophene-2-carboxylate;Ethyl 5-chloro-4-nitrothiophene-2-carboxylate
CAS:57800-76-7
MF:C6H4ClNO4S
MW:221.62
EINECS:
Product Categories:API intermediates
Mol File:57800-76-7.mol
5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER Structure
5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER Chemical Properties
Melting point 83-84 °C
Boiling point 349.3±37.0 °C(Predicted)
density 1.576±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
AppearanceWhite to light brown Solid
Safety Information
HS Code 2934999090
MSDS Information
5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER Usage And Synthesis
Synthesis
Methyl-5-chlorothiophene-2-carboxylate

35475-03-7

5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER

57800-76-7

Step 2: Preparation of methyl 5-chloro-4-nitrothiophene-2-carboxylate Fuming nitric acid (15 mL) was placed in an ice bath and cooled with saturated brine. Methyl 5-chlorothiophene-2-carboxylate (4.99 g, 28.3 mmol) was added slowly in small batches to avoid violent reaction. After addition, the reaction mixture was stirred in an ice bath for 1 hour. Upon completion of the reaction, the mixture was poured into ice water and a solid was precipitated. The precipitate was collected by filtration, washed with water and dried under vacuum to afford methyl 5-chloro-4-nitrothiophene-2-carboxylate (3.88 g, 58% yield). The product was characterized by 1H-NMR (400 MHz, DMSO-d6): δ 8.17 (1H, s).

References[1] Patent: EP1688420, 2006, A1. Location in patent: Page/Page column 122
[2] Patent: CN107903208, 2018, A. Location in patent: Paragraph 0136; 0137; 0139
[3] Journal of the American Chemical Society, 1952, vol. 74, p. 2965,2969
5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER Preparation Products And Raw materials
Raw materialsMethanol-->Methyl-5-chlorothiophene-2-carboxylate-->5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID
Tag:5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER(57800-76-7) Related Product Information
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