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107952-07-8

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107952-07-8 Usage

Chemical structure

2,4-Dihydro-4-(3-chlorophenyl)-5-((2-methoxyphenoxy)methyl)-3H-1,2,4-triazole-3-thione contains a 1,2,4-triazole ring, a thione group, a chlorophenyl group, and a methoxyphenoxy moiety.

Type of compound

It is a synthetic fungicide.

Application

Used in agriculture to control fungal diseases in various crops.

Mode of action

Inhibits the growth of fungi and prevents the spread of infections.

Potential biological activity

Studied for its possible anti-cancer and anti-inflammatory properties.

Safety concerns

Careful monitoring of use and handling is required due to potential toxicity and environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 107952-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,9,5 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107952-07:
(8*1)+(7*0)+(6*7)+(5*9)+(4*5)+(3*2)+(2*0)+(1*7)=128
128 % 10 = 8
So 107952-07-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H14ClN3O2S/c1-21-13-7-2-3-8-14(13)22-10-15-18-19-16(23)20(15)12-6-4-5-11(17)9-12/h2-9H,10H2,1H3,(H,19,23)

107952-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-chlorophenyl)-3-[(2-methoxyphenoxy)methyl]-1H-1,2,4-triazole-5-thione

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:107952-07-8 SDS

107952-07-8Downstream Products

107952-07-8Relevant articles and documents

Synthesis of Some New Substituted Mercaptotriazoles and Thiazolidones and Their Monoamine Oxidase Inhibitory and Anticonvulsant Properties

Husain, M. I.,Amir, Mohd,Singh, Eira

, p. 251 - 254 (2007/10/02)

A number of 4-aryl-5-aryloxymethyl-3-mercapto-1,2,4(H)-triazoles (IV) and 2-arylimino-3-aryloxyacetamido-4-thiazolidones (V) have been synthesized.Some of these compounds inhibit rat brain monoamine oxidase (MAO) in vitro at a final concentration of 1E-3 mol/litre, but are found to be inactive against pentylenetetrazole induced seizures in mice at a dose of 80 mg/kg.

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