ChemicalBook--->CAS DataBase List--->57800-76-7

57800-76-7

57800-76-7 Structure

57800-76-7 Structure
IdentificationBack Directory
[Name]

5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER
[CAS]

57800-76-7
[Synonyms]

AKOS 91745
Ethyl 5-chloro-4-nitrothiophene-2-carboxylate
Methyl 5-chloro-4-nitrothiophene-2-carboxylate
Methyl 5-chloro-4-nitro-2-thiophenecarboxylate
5-Chlor-4-nitro-2-thiophencarbonsaeureMethylester
5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER
2-Thiophenecarboxylic acid, 5-chloro-4-nitro-, methyl ester
5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER, 95+%
[Molecular Formula]

C6H4ClNO4S
[MDL Number]

MFCD08275718
[MOL File]

57800-76-7.mol
[Molecular Weight]

221.62
Chemical PropertiesBack Directory
[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
[Appearance]

White to light brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

5-CHLORO-4-NITROTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER(57800-76-7)1HNMR
Hazard InformationBack Directory
[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
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