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Benzene, 1-methyl-4-[[3-(methylthio)-2-propenyl]sulfonyl]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95526-71-9

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95526-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95526-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,5,2 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95526-71:
(7*9)+(6*5)+(5*5)+(4*2)+(3*6)+(2*7)+(1*1)=159
159 % 10 = 9
So 95526-71-9 is a valid CAS Registry Number.

95526-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-(methylthio)-3-(p-tolylsulfonyl)-1-propene

1.2 Other means of identification

Product number -
Other names 3-(methylthio)-2-propen-1-yl p-tolyl sulfone

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:95526-71-9 SDS

95526-71-9Relevant academic research and scientific papers

Radical-induced 1,3-Rearrangemets of Allylic Sulfones bearing an Alkylthio or Arylthio Substituent at the α-Position

Fox, Judith M.,Morris, Clare M.,Smyth, G. Darren,Whitman, Gordon H.

, p. 731 - 738 (2007/10/02)

1-Methylthio-1-p-tolylsulfonylprop-2-ene 2 underwent 1,3-rearrangement under conditions of radical initiation with migration of the p-tolylsulfonyl group by a process considered to have involved addition-elimination of arylsulfonyl radicals.In contrast, t

"Syn-Effect" in the Conversion of (E)-Vinylic Sulfones to the Corresponding Allylic Sulfones

Hirata, Takaki,Sasada, Yoshihiro,Ohtani, Takashi,Asada, Takahiro,Kinoshita, Hideki,et al.

, p. 75 - 96 (2007/10/02)

It was found that (E)-vinylic sulfones preferentially afford (Z)-allylic sulfones as kinetically-controlled products by treatment with a base under mild conditions, while (Z)-vinylic sulfones give (E)-allylic sulfones.Such stereochemical relationship was

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