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182257-03-0

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182257-03-0 Usage

General Description

2-Chloro-N,6-dimethyl-3-nitropyridin-4-amine is a chemical compound with the molecular formula C7H8ClN3O2. It is a nitropyridine derivative with a chlorine atom attached to the second carbon atom, two methyl groups attached to the sixth carbon atom, and a nitro group attached to the third carbon atom. 2-CHLORO-N,6-DIMETHYL-3-NITROPYRIDIN-4-AMINE is often used in the synthesis of pharmaceuticals and other organic compounds, and it may have potential applications in the field of medicinal chemistry. Its properties and potential uses make it a valuable and versatile chemical compound in various industries and research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 182257-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,2,5 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 182257-03:
(8*1)+(7*8)+(6*2)+(5*2)+(4*5)+(3*7)+(2*0)+(1*3)=130
130 % 10 = 0
So 182257-03-0 is a valid CAS Registry Number.

182257-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-CHLORO-N,6-DIMETHYL-3-NITROPYRIDIN-4-AMINE

1.2 Other means of identification

Product number -
Other names 2-chloro-N-6-dimethyl-3-nitro-pyridin-4-amine

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:182257-03-0 SDS

182257-03-0Relevant articles and documents

2-n-butyl-9-methyl-8-[1,2,3]triazol-2-yl-9H-purin-6-ylamine and analogues as A2A adenosine receptor antagonists. Design, synthesis, and pharmacological characterization

Minetti, Patrizia,Tinti, Maria Ornella,Carminati, Paolo,Castorina, Massimo,Di Cesare, Maria Assunta,Di Serio, Stefano,Gallo, Grazia,Ghirardi, Orlando,Giorgi, Fabrizio,Giorgi, Luca,Piersanti, Giovanni,Bartoccini, Francesca,Tarzia, Giorgio

, p. 6887 - 6896 (2007/10/03)

Two types of adenosine receptor ligands were designed, i.e., 9H-purine and 1H-imidazo[4,5-c]pyridines, to obtain selective A2A antagonists, and we report here their synthesis and binding affinities for the four adenosine receptor subtypes Asub

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