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13099-56-4

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13099-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13099-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,9 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13099-56:
(7*1)+(6*3)+(5*0)+(4*9)+(3*9)+(2*5)+(1*6)=104
104 % 10 = 4
So 13099-56-4 is a valid CAS Registry Number.

13099-56-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-(1-chloro-2-methylpropan-2-yl)benzene

1.2 Other means of identification

Product number -
Other names 4-Chlor-neophylchlorid

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:13099-56-4 SDS

13099-56-4Relevant articles and documents

-

Harvey,L. et al.

, p. 5019 - 5026 (1969)

-

2-Arylpropyl ether or thioether derivatives and insecticidal and acaricidal agents containing said derivatives

-

, (2008/06/13)

The present invention relates to 2-arylpropyl ether or thioether derivatives represented by the following general formula [I]: STR1 wherein Ar stands for an aryl group, R stands for a methyl or ethyl group, Y stands for an oxygen or sulfur atom, and B stands for a group represented by the following formula [II]: STR2 or the following general formula [III]: STR3 wherein Z stands for an oxygen or sulfur atom or a carbonyl or methylene group, R1 stands for a hydrogen or halogen atom or a lower alkyl group or a lower alkoxy group, and n is an integer of from 1 to 5 with the proviso that when n is 2 or more, the groups R1 may be the same or different, and also to processes for the preparation or these ethers of thioethers and a use of these ethers or thioethers. These compounds of the present invention have excellent insecticidal and acaricidal activities while the toxicity of these compounds are very low.

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