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5-Nitrothiophene-2-carboxamide is a chemical compound with the molecular formula C5H4N2O3S. It is a derivative of thiophene, a heterocyclic compound consisting of a benzene ring with one sulfur atom replacing a carbon atom. The 5-nitro group is attached to the thiophene ring, and the 2-carboxamide functional group is present at the second carbon position. 5-nitrothiophene-2-carboxamide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of other organic compounds. Due to its reactivity and functional groups, 5-nitrothiophene-2-carboxamide is a versatile building block in organic chemistry, particularly in the development of new drugs and chemical products.

5832-00-8

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5832-00-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5832-00-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5832-00:
(6*5)+(5*8)+(4*3)+(3*2)+(2*0)+(1*0)=88
88 % 10 = 8
So 5832-00-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N2O3S/c6-5(8)3-1-2-4(11-3)7(9)10/h1-2H,(H2,6,8)

5832-00-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-nitrothiophene-2-carboxamide

1.2 Other means of identification

Product number -
Other names CCG-1823

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5832-00-8 SDS

5832-00-8Relevant academic research and scientific papers

SUBSTITUTED OXOPYRIDINE DERIVATIVES

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Paragraph 0486; 0487; 0500-0503, (2018/05/24)

The invention relates to substituted oxopyridine derivatives and to processes for preparation thereof, and also to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases, especially of cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

INHIBITORS OF JANUS KINASES

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Page/Page column 102, (2009/01/23)

The instant invention provides for compounds that inhibit the four known mammalian JAK kinases (JAK1, JAK2, JAK3 and TYK2) and PDK1. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting the activity of JAK1, JAK2, JAK3 TYK2 and PDK1 by administering the compound to a patient in need of treatment for myeloproliferative disorders or cancer.

Labelled compounds of interest as antitumour agents - VI. Isotopically efficient syntheses of [15N]-nitrothiophenecarboxamides

Shinkwin, Anne E.,Threadgill, Michael D.

, p. 1015 - 1020 (2007/10/03)

Reaction of 3-cyanothiophene with one equivalent of potassium nitrate in concentrated sulphuric acid causes nitration, concurrent with hydrolysis of the nitrile, to give 5-nitro-thiophene-3-carboxamide in high yield. Similarly, 2-cyanothiophene gives 4-nitro-thiophene-2-carboxamide and 5-nitrothiophene-2-carboxamide, benzonitrile gives 3-nitrobenzamide and 4-methylbenzonitrile gives 4-methyl-3-nitrobenzamide. Extension of this process to use of potassium [15N]-nitrate, formed from [15N]-nitric acid (95% isotopic enrichment), enables preparation of the corresponding [15N]-nitrothiophenecarboxamides in high isotopic yield.

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