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129768-95-2

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129768-95-2 Usage

Description

(4-METHYLPYRIDIN-2-YL)METHYLAMINE, with the molecular formula C7H10N2, is a versatile chemical compound belonging to the pyridine family, a class of nitrogen-containing heterocycles. Its structure features both an amine and a pyridine group, which allows it to form various types of chemical bonds and interact with a broad spectrum of other compounds, making it a valuable chemical intermediate in the chemical industry.

Uses

Used in Pharmaceutical Synthesis:
(4-METHYLPYRIDIN-2-YL)METHYLAMINE is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure enables it to be incorporated into complex molecular frameworks, enhancing the properties and effectiveness of the resulting pharmaceuticals.
Used in Organic Compounds Synthesis:
In the realm of organic chemistry, (4-METHYLPYRIDIN-2-YL)METHYLAMINE serves as a key component in the synthesis of a wide range of organic compounds. Its presence in these compounds can influence their reactivity, stability, and overall performance, making it an essential ingredient in the creation of novel organic materials.
Used in Coordination Chemistry:
(4-METHYLPYRIDIN-2-YL)METHYLAMINE is employed as a ligand in coordination chemistry, where it forms coordination complexes with metal ions. These complexes have potential applications in catalysis, materials science, and as models for understanding biological systems, showcasing the compound's versatility in chemical interactions.
Used in Agrochemical Production:
As a precursor in the production of agrochemicals, (4-METHYLPYRIDIN-2-YL)METHYLAMINE plays a crucial role in the development of pesticides, herbicides, and other agricultural chemicals. Its incorporation into these compounds can lead to improved efficacy, selectivity, and environmental compatibility, supporting sustainable agricultural practices.
Used in Fine Chemicals Industry:
(4-METHYLPYRIDIN-2-YL)METHYLAMINE is utilized as a starting material in the synthesis of fine chemicals, which are high-purity, specialty chemicals used in various industries such as fragrances, dyes, and flavorings. Its presence in these products can enhance their quality and performance, making it an indispensable component in the fine chemicals sector.

Check Digit Verification of cas no

The CAS Registry Mumber 129768-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,6 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 129768-95:
(8*1)+(7*2)+(6*9)+(5*7)+(4*6)+(3*8)+(2*9)+(1*5)=182
182 % 10 = 2
So 129768-95-2 is a valid CAS Registry Number.

129768-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylpyridin-2-yl)methanamine

1.2 Other means of identification

Product number -
Other names (4-methyl-2-pyridyl)methanamine

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:129768-95-2 SDS

129768-95-2Upstream product

129768-95-2Downstream Products

129768-95-2Relevant articles and documents

PRODUCTION METHOD OF OPTICALLY ACTIVE SECONDARY ALCOHOL

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Paragraph 0127; 0129, (2016/11/14)

PROBLEM TO BE SOLVED: To provide a chemical catalytic method allowing efficient production of a corresponding optically active secondary alcohol from an aromatic ketone having a substituent at each of two β-positions in an aromatic ring to the carbonyl site, so that both enantiomers can be separately made. SOLUTION: A production method of optically active secondary alcohol is characterized by reacting a ketone compound such as acetophenone derivatives with hydrogen in the presence of a ruthenium complex catalyst having an optically active diphosphine ligand. COPYRIGHT: (C)2015,JPO&INPIT

ARYL FLUOROETHYL UREAS ACTING AS ALPHA 2 ADRENERGIC AGENTS

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Page/Page column 31, (2008/12/07)

The invention provides well-defined aryl fluoroethyl ureas that are useful as selective alpha2 adrenergic agonists. As such, the compounds described herein are useful in treating a wide variety of disorders associated with modulation of alpha2 adrenergic receptors.

N-Acylated azacyclic compounds, processes for their preparations and their use as medications

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, (2008/06/13)

A compound, or a solvate or salt thereof, of formula (I): in which: RCO is an acyl group in which the group R contains a substituted or unsubstituted carbocyclic aromatic or heterocyclic aromatic ring; R? and R? are independently hydrogen, C??? alkyl, C??

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