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5424-92-0

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5424-92-0 Usage

Group

Organochlorine compounds

Usage

Widely used in the production of pesticides and other industrial chemicals

Application

Potent insecticide and acaricide for controlling pests in agricultural, commercial, and residential settings

Mechanism of Action

Acts as a cholinesterase inhibitor, disrupting the normal functioning of the nervous system in insects and mites

Potential Toxicity

Toxic to humans and other non-target organisms

Regulation

Use is strictly regulated in many countries due to its potential toxicity

Check Digit Verification of cas no

The CAS Registry Mumber 5424-92-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5424-92:
(6*5)+(5*4)+(4*2)+(3*4)+(2*9)+(1*2)=90
90 % 10 = 0
So 5424-92-0 is a valid CAS Registry Number.

5424-92-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-[(4-chlorophenyl)methylsulfanylmethylsulfanylmethyl]benzene

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:5424-92-0 SDS

5424-92-0Downstream Products

5424-92-0Relevant articles and documents

Reduction of CO2 into Methylene Coupled with the Formation of C-S Bonds under NaBH4/I2 System

Guo, Zhiqiang,Zhang, Bo,Wei, Xuehong,Xi, Chanjuan

supporting information, p. 6678 - 6681 (2018/10/24)

A selective four-electron reduction of CO2 with thiophenol using NaBH4 as a reductant is described to access dithioacetals. This reaction provides a novel synthetic method for the highly selective conversion of CO2 into methylene, and a new access to molecular structures via formation of C-S bonds using CO2 as the C1 source.

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