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4093-89-4

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4093-89-4 Usage

General Description

2-Methylamino-5-nitropyridine is a chemical compound with the molecular formula C6H7N3O2. It is a yellow crystalline solid with a molecular weight of 153.14 g/mol. 2-METHYLAMINO-5-NITROPYRIDINE is primarily used in the pharmaceutical industry as an intermediate for the synthesis of various drugs and other organic compounds. It is also used as a building block for the production of specialty chemicals and agrochemicals. 2-Methylamino-5-nitropyridine is considered to be a hazardous substance and should be handled with care due to its toxic and potentially harmful properties.

Check Digit Verification of cas no

The CAS Registry Mumber 4093-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,9 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4093-89:
(6*4)+(5*0)+(4*9)+(3*3)+(2*8)+(1*9)=94
94 % 10 = 4
So 4093-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O2/c1-7-6-3-2-5(4-8-6)9(10)11/h2-4H,1H3,(H,7,8)

4093-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Methylamino)-5-nitropyridine

1.2 Other means of identification

Product number -
Other names 2-METHYLAMINO-5-NITROPYRIDINE

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:4093-89-4 SDS

4093-89-4Relevant articles and documents

Oxidative Methylamination of Some Nitropyridines

Szpakiewicz, Barbara,Wozniak, Marian

, p. 75 - 78 (2007/10/03)

2-, 3-, 4-Nitropyridine (1a, i, j) and some simple derivatives of 3-nitropyridine (1b-h) undergo dehydromethylamination in a solution of potassium permanganate in liquid methylamine. In the case of 2- and 6-chloro and 6-methoxy derivatives of 3-nitropyridine (1b-d) dechloro- or demethoxy-methylamination occurs as well.

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