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(4-CHLORO-PYRIDIN-2-YL)-DIMETHYL-AMINE, with the molecular formula C7H9ClN2, is an organic compound characterized by a chloro-substituted pyridine ring and a dimethylamine group. It is recognized for its versatility and value as a key intermediate in the synthesis of a diverse array of products, including pharmaceuticals, agrochemicals, and other organic compounds.

735255-56-8

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735255-56-8 Usage

Uses

Used in Pharmaceutical Industry:
(4-CHLORO-PYRIDIN-2-YL)-DIMETHYL-AMINE is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of molecules with specific biological activities, making it a valuable component in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, (4-CHLORO-PYRIDIN-2-YL)-DIMETHYL-AMINE is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds, thereby supporting agricultural productivity.
Used as a Reagent in Chemical Reactions:
(4-CHLORO-PYRIDIN-2-YL)-DIMETHYL-AMINE serves as a reagent in various chemical reactions, facilitating the synthesis of complex organic molecules. Its presence can influence reaction pathways and outcomes, making it an essential tool in organic synthesis.
Used as a Catalyst in Organic Synthesis:
Furthermore, (4-CHLORO-PYRIDIN-2-YL)-DIMETHYL-AMINE is employed as a catalyst to accelerate organic synthesis processes. Its ability to lower activation energy and increase reaction rates is beneficial in the production of a wide range of organic compounds, enhancing the efficiency of synthetic processes across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 735255-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,5,2,5 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 735255-56:
(8*7)+(7*3)+(6*5)+(5*2)+(4*5)+(3*5)+(2*5)+(1*6)=168
168 % 10 = 8
So 735255-56-8 is a valid CAS Registry Number.

735255-56-8SDS

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 4-chloro-N,N-dimethylpyridin-2-amine

1.2 Other means of identification

Product number -
Other names 4-chloro-2-dimethylaminopyridine hydrochloride

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:735255-56-8 SDS

735255-56-8Downstream Products

735255-56-8Relevant academic research and scientific papers

Nucleophilic Aromatic Substitution Reactions in Water Enabled by Micellar Catalysis

Isley, Nicholas A.,Linstadt, Roscoe T. H.,Kelly, Sean M.,Gallou, Fabrice,Lipshutz, Bruce H.

supporting information, p. 4734 - 4737 (2015/10/12)

Given the huge dependence on dipolar, aprotic solvents such as DMF, DMSO, DMAc, and NMP in nucleophilic aromatic substitution reactions (SNAr), a simple and environmentally friendly alternative is reported. Use of a "benign-by-design" nonionic surfactant, TPGS-750-M, in water enables nitrogen, oxygen, and sulfur nucleophiles to participate in SNAr reactions. Aromatic and heteroaromatic substrates readily participate in this micellar catalysis, which takes place at or near ambient temperatures.

DIARYLAMINE-SUBSTITUTED QUINOLONES USEFUL AS INDUCIBLE NITRIC OXIDE SYNTHASE INHIBITORS

-

Page/Page column 47, (2009/04/25)

Novel diarylamine-substituted quinolone compounds and pharmaceutical compositions, certain of which have been found to inhibit inducible NOS synthase have been discovered, together with methods of synthesizing and using the compounds including methods for the treatment of iNOS-mediated diseases in a patient by administering the compounds.

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