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[2-(Methylsulfinyl)ethenyl]benzene, also known as 2-(methylsulfinyl)styrene or methylsulfinylstyrene, is an organic compound with the chemical formula C9H10OS. It is a colorless to pale yellow liquid with a pungent odor. [2-(Methylsulfinyl)ethenyl]benzene is characterized by the presence of a methylsulfinyl group (CH3SO) attached to a vinyl group (C=CH2), which is in turn connected to a benzene ring. It is used as an intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Due to its reactivity, it is important to handle this chemical with care, following proper safety protocols.

7715-00-6

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7715-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7715-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7715-00:
(6*7)+(5*7)+(4*1)+(3*5)+(2*0)+(1*0)=96
96 % 10 = 6
So 7715-00-6 is a valid CAS Registry Number.

7715-00-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylsulfinylethenylbenzene

1.2 Other means of identification

Product number -
Other names 1-Methylsulfinyl-2-phenyl-ethylen

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:7715-00-6 SDS

7715-00-6Relevant academic research and scientific papers

CoCl2 catalysed decarboxylation-oxidation of mandelic acids by molecular oxygen

Favier, Isabelle,Dunach, Elisabet,Hebrault, Dominique,Desmurs, Jean-Roger

, p. 62 - 66 (2007/10/03)

A series of mandelic acid derivatives was oxidised by molecular oxygen using cobalt(II) chloride as the catalyst. Benzaldehyde and/or benzoic acid derivatives were obtained in high selectivities, depending on the aromatic ring substitution. Different oxidation mechanisms are operating, depending on the mandelic acid substitution.

The reactions of DMSO with arylaldehydes in the presence of sodium hydride

Shi, Min,Shen, Yu-Mei

, p. 422 - 427 (2007/10/03)

Dimethyl sulfoxide (DMSO) reacted with arylaldehydes under basic conditions to afford sulfide 1, β-(benzyloxy)styrene 2 and dialkyl sulfoxide 3, while the reaction of benzophenone with DMSO gave 1,1-diphenylethylene 4, 1,1-diphenyl-2-methylthioethylene 5 and sulfoxide 6 at the same time under the same conditions.

Selective synthesis of cis-α,β-unsaturated sulfoxides and sulfides by the Horner-Wittig reaction with bis(2,2,2-trifluoroethyl)phosphono sulfoxides and aromatic aldehydes

Kokin, Keisuke,Tsuboi, Shuji,Motoyoshiya, Jiro,Hayashi, Sadao

, p. 637 - 640 (2007/10/03)

cis-α,β-Unsaturated sulfoxides were predominantly formed in the Horner-Wittig reaction with bis(2,2,2-trifluoroethyl)phosphono sulfoxides and aromatic aldehydes, while the reaction of the corresponding sulfides showed trans- or lower cis-selectivity. The reduction of cis-α,β-unsaturated sulfoxides with tributylphosphine in carbon tetrachloride gave cis-vinyl sulfides with retention of stereochemistry.

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