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28033-03-6

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28033-03-6 Usage

General Description

Methyl 2-amino-5-nitroisonicotinate is a chemical compound with the molecular formula C7H7N3O4. It is a derivative of isonicotinic acid and contains a methyl group, an amino group, and a nitro group. Methyl 2-aMino-5-nitroisonicotinate is used in organic synthesis and pharmaceutical research, particularly in the development of antituberculosis drugs. It has also been investigated for its potential anticancer and antimicrobial properties. Methyl 2-amino-5-nitroisonicotinate is a valuable intermediate in the synthesis of various biologically active compounds and has potential applications in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 28033-03-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,3 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28033-03:
(7*2)+(6*8)+(5*0)+(4*3)+(3*3)+(2*0)+(1*3)=86
86 % 10 = 6
So 28033-03-6 is a valid CAS Registry Number.

28033-03-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-amino-5-nitropyridine-4-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 2-amino-5-nitroisonicotinate

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:28033-03-6 SDS

28033-03-6Downstream Products

28033-03-6Relevant articles and documents

Selective vicarious nucleophilic amination of 3-nitropyridines

Bakke, Jan M.,Svensen, Harald,Trevisan, Raffaela

, p. 376 - 378 (2007/10/03)

Nine 3-nitropyridine compounds and 4-nitroisoquinoline have been aminated in the 6-position (for 4-nitroisoquinoline in the 1-position) by vicarious nucleophilic substitution reactions. Two amination reagents were used, hydroxylamine and 4-amino-1,2,4-triazole. The yields were from moderate to good. Use of hydroxylamine gave an easy work-up procedure by which almost pure product was obtained directly, but 4-amino-1,2,4-triazole gave better yields of the aminated product for some of the substrates. By this, a general method for the preparation of 3- or 4-substituted-2-amino-5-nitropyridines was obtained.

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