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2-Chloro-N4,6-dimethylpyridine-3,4-diamine is a chemical compound that belongs to the class of organic compounds known as aminopyridines and derivatives. These are organic compounds containing an amino group attached to a pyridine ring. This particular compound has two methyl groups substituting the 4 and 6 positions of the pyridine ring, an amine group each at both the 3 and 4 positions, and a chlorine atom at the 2 position. 2-CHLORO-N4,6-DIMETHYLPYRIDINE-3,4-DIAMINE, known by its CAS registry number 73992-70-8, is typically a solid and is used in various scientific and industrial applications. Details such as its molecular weight, exact chemical structure, or physicochemical properties would depend on available data and other specific factors. It should be handled with appropriate safety measures due to potential reactivity or toxicity.

870135-16-3

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870135-16-3 Usage

Uses

Used in Chemical Synthesis:
2-Chloro-N4,6-dimethylpyridine-3,4-diamine is used as a chemical intermediate for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a wide range of derivatives with potential applications in different industries.
Used in Research Applications:
In the field of scientific research, 2-Chloro-N4,6-dimethylpyridine-3,4-diamine is used as a reagent or starting material for the development of new compounds with specific properties. Its versatility in chemical reactions makes it a valuable tool for researchers exploring new chemical pathways and potential applications.
Used in Pharmaceutical Industry:
2-Chloro-N4,6-dimethylpyridine-3,4-diamine is used as a building block in the development of new drugs. Its presence in the molecular structure can influence the pharmacological properties of the final product, such as solubility, stability, and bioavailability, making it an important component in the design of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloro-N4,6-dimethylpyridine-3,4-diamine is used as a precursor for the synthesis of pesticides and other crop protection products. Its incorporation into these compounds can contribute to their effectiveness in controlling pests and diseases, ultimately benefiting agricultural productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 870135-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,1,3 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 870135-16:
(8*8)+(7*7)+(6*0)+(5*1)+(4*3)+(3*5)+(2*1)+(1*6)=153
153 % 10 = 3
So 870135-16-3 is a valid CAS Registry Number.

870135-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-N,6-dimethylpyridine-3,4-diamine

1.2 Other means of identification

Product number -
Other names 2-chloro-6,N4-dimethylpyridine-3,4-diamine

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:870135-16-3 SDS

870135-16-3Relevant academic research and scientific papers

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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