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Benzene, 1-[(2-methylphenyl)methyl]-2-[(2-methylphenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88790-16-3

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88790-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88790-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,9 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88790-16:
(7*8)+(6*8)+(5*7)+(4*9)+(3*0)+(2*1)+(1*6)=183
183 % 10 = 3
So 88790-16-3 is a valid CAS Registry Number.

88790-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzene, 1-[(2-methylphenyl)methyl]-2-[(2-methylphenyl)thio]-

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:88790-16-3 SDS

88790-16-3Upstream product

88790-16-3Downstream Products

88790-16-3Relevant academic research and scientific papers

REACTION OF DIMETHYL SULFITE WITH PHENYLLITHIUM. FORMATION OF BIPHENYL AND DIPHENYL SULFIDE VIA SULFURANE

Hara, Yoshinori,Matsuda, Minoru

, p. 211 - 222 (2007/10/02)

Dimethyl sulfite reacted an excess of phenyllithium yielding biphenyl and diphenyl sulfide in good yield.Other dialkyl sulfites also reacted giving identical yields of biphenyl and diphenyl sulfide irrespective of the structure of the aryl groups, indicating that dialkyl sulfites can be used for the reaction with aryllithiums in place of diaryl sulfoxides.The mechanism of the reaction of diaryl sulfoxides with aryllithium is discussed on the the basis of the isomer distribution of bitolyls, the effect of additives, and the ratio of the benzyne and sulfonium salt pathways.Sulfurane 1 is formed in an initial stage of the reaction of diaryl sulfoxide with aryllithium followed by its competitive collapse by way of benzyne and sulfonium salt pathways.

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