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6317-37-9

6317-37-9 Structure

6317-37-9 Structure
IdentificationMore
[Name]

5-Nitrothiophene-2-carboxylic acid
[CAS]

6317-37-9
[Synonyms]

5-Nitro-2-thenoic acid
5-NITRO-2-THIOPHENECARBOXYLIC ACID
5-NITROTHIOPHENE-2-CARBOXYLIC ACID
BUTTPARK 121\04-13
RARECHEM AL BO 0544
5-Nitro-2-ThiphenecarboxylicAcid
5-nitro-2-thiophenecarboxylic
[EINECS(EC#)]

228-654-4
[Molecular Formula]

C5H3NO4S
[MDL Number]

MFCD00159552
[Molecular Weight]

173.15
[MOL File]

6317-37-9.mol
Chemical PropertiesBack Directory
[Melting point ]

154-159℃
[Boiling point ]

367.2±27.0 °C(Predicted)
[density ]

1.676±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

Solid
[pka]

2.69±0.10(Predicted)
[color ]

Pale yellow
[InChIKey]

UNEPVPOHGXLUIR-UHFFFAOYSA-N
[CAS DataBase Reference]

6317-37-9(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Safety Statements ]

24/25
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HS Code ]

29349990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Acetic acid-->Nitric acid-->Acetic anhydride-->2-Thiophenecarboxylic acid-->5-Nitrothiophene-2-carboxaldehyde-->Sodium chlorite-->Water-->Sulfamic acid-->1,4-Dioxane
[Preparation Products]

5-Amino-thiophene-2-carboxylic acid methyl ester
Hazard InformationBack Directory
[Chemical Properties]

Solid
[Uses]

5-Nitrothiophene-2-carboxylic Acid is a reagent used in the preparation of benzothiophene amides which fuctions as nicotinamide ribosyltransferase inhibitors with potential antitumor and anticancer activities. It also functions as an intermediate in varying organic transformations.
[Synthesis Reference(s)]

Canadian Journal of Chemistry, 44, p. 2881, 1966 DOI: 10.1139/v66-428
Journal of Medicinal Chemistry, 34, p. 2112, 1991
[Synthesis]

5-NITROTHIOPHENE-2-CARBOXALDEHYDE

4521-33-9

5-Nitrothiophene-2-carboxylic acid

6317-37-9

General procedure for the synthesis of 5-nitrothiophene-2-carboxylic acid from 5-nitrothiophene-2-carboxaldehyde: 5-nitrothiophene-2-carboxaldehyde (1.685 g, 10.72 mmol) was dissolved in dioxane (30 mL) with sulfamic acid (1.249 g, 12.87 mmol) and cooled down to 0 °C. Subsequently, an aqueous solution of sodium chlorite (1.940 g, 21.44 mmol) was added slowly and dropwise (14 mL). The reaction mixture was gradually warmed to room temperature and stirred continuously for 2 hours. A second batch of 5-nitrothiophene-2-carbaldehyde (1.966 g, 12.51 mmol) was treated at the same molar ratio under the same conditions. The two reaction mixtures were combined and extracted by partitioning with ethyl acetate and water. The organic phase was extracted twice with 5% NaHCO3 solution and discarded. The basic aqueous phase was adjusted to pH=2 with 2N HCl and extracted twice with ethyl acetate. The organic layers were combined, washed with brine and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure to give 5-nitrothiophene-2-carboxylic acid (Int.53) (3.6 g, 20.79 mmol, MS/ESI+ 173.9 [MH]+).

[References]

[1] Patent: US4220793, 1980, A
[2] Patent: US4220793, 1980, A
[3] Patent: US4220793, 1980, A
[4] Patent: WO2004/18480, 2004, A1. Location in patent: Page 155
[5] Helvetica Chimica Acta, 2002, vol. 85, # 12, p. 4485 - 4517
Spectrum DetailBack Directory
[Spectrum Detail]

5-Nitrothiophene-2-carboxylic acid(6317-37-9)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

6317-37-9(sigmaaldrich)
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