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92289-44-6

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92289-44-6 Usage

Description

1-(5-Methyl-1-phenyl-1H-1,2,4-triazol-3-yl)ethanone, also known as MET, is a chemical compound with the molecular formula C10H10N2O. It is a ketone derivative, and its structure consists of a 1,2,4-triazole ring attached to a phenyl group and a methyl group. MET has been studied for its potential pharmacological properties, including its potential use as a central nervous system stimulant and its antidepressant and anxiolytic effects. It has also been investigated for its potential role in the treatment of neurodegenerative diseases. Additionally, MET has been used as a precursor in the synthesis of other organic compounds.

Uses

Used in Pharmaceutical Industry:
1-(5-Methyl-1-phenyl-1H-1,2,4-triazol-3-yl)ethanone is used as a central nervous system stimulant for its potential to enhance cognitive function and alertness.
1-(5-Methyl-1-phenyl-1H-1,2,4-triazol-3-yl)ethanone is used as an antidepressant for its potential to alleviate symptoms of depression by modulating neurotransmitter levels in the brain.
1-(5-Methyl-1-phenyl-1H-1,2,4-triazol-3-yl)ethanone is used as an anxiolytic for its potential to reduce anxiety and stress by affecting the central nervous system.
1-(5-Methyl-1-phenyl-1H-1,2,4-triazol-3-yl)ethanone is used in the treatment of neurodegenerative diseases for its potential neuroprotective effects and ability to slow down the progression of these diseases.
Used in Chemical Synthesis:
1-(5-Methyl-1-phenyl-1H-1,2,4-triazol-3-yl)ethanone is used as a precursor in the synthesis of other organic compounds for its ability to form various chemical structures and contribute to the development of new pharmaceuticals and other chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 92289-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,8 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92289-44:
(7*9)+(6*2)+(5*2)+(4*8)+(3*9)+(2*4)+(1*4)=156
156 % 10 = 6
So 92289-44-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N3O/c1-8(15)11-12-9(2)14(13-11)10-6-4-3-5-7-10/h3-7H,1-2H3

92289-44-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-methyl-1-phenyl-1,2,4-triazol-3-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-Phenyl-5-methyl-3-acetyl-1,2,4-triazol

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:92289-44-6 SDS

92289-44-6Downstream Products

92289-44-6Relevant articles and documents

One-flask synthesis of 1,3,5-trisubstituted 1,2,4-triazoles from nitriles and hydrazonoyl chlorides via 1,3-dipolar cycloaddition

Wang, Li-Ya,Tsai, Henry J.,Lin, Hui-Yi,Kaneko, Kimiyoshi,Cheng, Fen-Ying,Shih, Hsin-Siao,Wong, Fung Fuh,Huang, Jiann-Jyh

, p. 14215 - 14220 (2014/04/17)

A one-flask strategy for the synthesis of 1,3,5-trisubstituted 1,2,4-triazoles 4a-s and 8a and b from nitriles 5a-i with N-arylhydrazonoyl hydrochlorides 3a-h and 7a and b under basic conditions was developed. The reaction provided the desired 1,2,4-triazoles in moderate to excellent yields (56-98%), and was applicable to aliphatic and aromatic nitriles as well as N-phenylhydrazonoyl hydrochlorides bearing ester and acetyl functionalities. A 1,3-dipolar cycloaddition between imidate and nitrilimine generated from the respective nitrile and N-arylhydrazonoyl chloride in one flask was proposed for the new transformation.

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