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114366-07-3

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114366-07-3 Usage

Description

2-Pyridinemethanamine,N,alpha-dimethyl-(9CI), also known as 2-Methyl-2-Pyridinemethylamine and 2-Dimethylaminomethylpyridine, is a chemical compound with the molecular formula C8H12N2. It is a tertiary amine characterized by the presence of a pyridine ring and a methyl group attached to the nitrogen atom. This versatile chemical structure and reactivity make it an important compound in various applications.

Uses

Used in Organic Synthesis:
2-Pyridinemethanamine,N,alpha-dimethyl-(9CI) is used as a reagent and catalyst in organic synthesis for its ability to facilitate various chemical reactions. Its unique structure allows it to participate in a wide range of reactions, making it a valuable component in the synthesis of numerous chemical compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Pyridinemethanamine,N,alpha-dimethyl-(9CI) is utilized for its potential applications in the development of new drugs. Its chemical properties enable it to interact with biological targets, making it a promising candidate for the creation of novel therapeutic agents.
Used in Agrochemical Industry:
2-Pyridinemethanamine,N,alpha-dimethyl-(9CI) also finds use in the agrochemical industry, where it is employed in the synthesis of various agrochemical products. Its reactivity and structural features contribute to the development of effective compounds for agricultural applications.
It is crucial to handle 2-Pyridinemethanamine,N,alpha-dimethyl-(9CI) with care and adhere to proper safety protocols, as it can pose hazards if not managed responsibly.

Check Digit Verification of cas no

The CAS Registry Mumber 114366-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,6 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 114366-07:
(8*1)+(7*1)+(6*4)+(5*3)+(4*6)+(3*6)+(2*0)+(1*7)=103
103 % 10 = 3
So 114366-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-7(9-2)8-5-3-4-6-10-8/h3-7,9H,1-2H3

114366-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-1-pyridin-2-ylethanamine

1.2 Other means of identification

Product number -
Other names -

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:114366-07-3 SDS

114366-07-3Relevant articles and documents

HETEROCYCLIC COMPOUNDS AS ADENOSINE ANTAGONISTS

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Paragraph 0214, (2020/10/31)

Aminopyrazine compounds as modulators of an adenosine receptor are provided. The compounds may find use as therapeutic agents for the treatment of diseases mediated through a G-protein-coupled receptor signaling pathway and may find particular use in onco

Compounds with Bridgehead Nitrogen 52 -NMR Spectra and Stereochemistry of the 2-Alkylperhydroimidazolopyridines

Banting, Lee,Crabb, Trevor A.

, p. 696 - 706 (2007/10/02)

In contrast to perhydro-oxazolopyridine and perhydrothiazolopyridine, which adopt equilibria in CDCl3 solution at room temperature containing ca 70percent trans-fused conformers in equilibria with O- or S-inside cis-fused conformers, 2-alkylperhydroimidazolopyridines are found to adopt equilibria containing >98percent trans-fused conformers.Comparison of NMR parameters of 2-methylperhydroimidazolopyridine with those of the two isomers of 1,2-dimethylperhydroimidazolopyridine indicates an equilibrium for the former compound between the two trans-fused conformers, with ca 83percent of that conformation containing a transarrangement of nitrogen lone pairs of electrons.These observations are explained in terms of the generalized anomeric effect.KEY WORDS Perhydroimidazolopyridine Conformational equilibria 1H and 13C NMR

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