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33245-29-3

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33245-29-3 Usage

General Description

5-Brom0-N-nitropyridin-2-amine is a chemical compound with the molecular formula C5H4BrN3O2. It is a nitroamine derivative with a bromine atom attached to the 5th position of the pyridine ring. 5-broMo-N-nitropyridin-2-aMine is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also utilized in the manufacture of dyes and organic compounds. 5-Brom0-N-nitropyridin-2-amine is known for its ability to undergo various chemical reactions, making it a versatile building block in organic synthesis. Due to its potential applications, this compound is of interest to researchers and chemical manufacturers.

Check Digit Verification of cas no

The CAS Registry Mumber 33245-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,4 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33245-29:
(7*3)+(6*3)+(5*2)+(4*4)+(3*5)+(2*2)+(1*9)=93
93 % 10 = 3
So 33245-29-3 is a valid CAS Registry Number.

33245-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(5-bromopyridin-2-yl)nitramide

1.2 Other means of identification

Product number -
Other names 5-bromo-2-nitraminopyridine

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:33245-29-3 SDS

33245-29-3Relevant articles and documents

Syntheses with Aromatic Nitramines. IX. Halogenation of 2- and 4-Nitraminopyridines

Brzozka, L.,Baran, W.,Kraus, W.,Tomasik, P.

, p. 605 - 611 (2007/10/02)

Isomeric 2- and 4-nitraminopyridines (free acids and anions) were subjected to halogenation (iodination, bromination and chlorination).The iodination of nitraminopyridine anions failed, and the bromination and chlorination led selectively to 5-monohalogenated products independently of whether free acids or anions of nitraminopyridines were reacted.Key words: nitraminopyridines, halogenation

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