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

72195-49-4

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72195-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72195-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,1,9 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72195-49:
(7*7)+(6*2)+(5*1)+(4*9)+(3*5)+(2*4)+(1*9)=134
134 % 10 = 4
So 72195-49-4 is a valid CAS Registry Number.

72195-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-4-(1-phenylbut-3-en-2-ylsulfonyl)benzene

1.2 Other means of identification

Product number -
Other names Benzene,1-methyl-4-[[1-(phenylmethyl)-2-propenyl]sulfonyl]

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:72195-49-4 SDS

72195-49-4Relevant academic research and scientific papers

Direct transformation of terminal alkynes to branched allylic sulfones

Xu, Kun,Khakyzadeh, Vahid,Bury, Timm,Breit, Bernhard

supporting information, p. 16124 - 16127 (2015/01/09)

A new strategy for the transformation of terminal alkynes to branched allylic sulfones was developed. Using a Rh(I)/DPEphos/benzoic acid catalyst system, terminal alkynes react with sulfonyl hydrazides to produce branched allylic sulfones with good to exc

Preparation of some Allylic Sulphones; Base-catalysed Isomerisation and Deuteriation of Cyclohex-2-enyl p-Tolyl Sulphones

Knight, Derek J.,Lin, Peter,Russell, Simon T.,Whitham, Gordon H.

, p. 2701 - 2706 (2007/10/02)

A summary of the methods used in the preparation of a range of allylic sulphones is given.In the case of the conformationally biased sulphones (5) and (6) stereospecific preparation from the cis- and trans-5-t-butylcyclohex-2-en-1-ols was achieved by rear

Synthesis of (+/-)-Lavandulol and its Related Homoallylic Alcohol via Allyl Transfer from Sulphur to Tin

Ueno, Yoshio,Aoki, Seiichi,Okawara, Makoto

, p. 683 - 684 (2007/10/02)

(+/-)-Lavandulol and related homoallylic alcohols were prepared by the stannolysis of allylic sulphones and the subsequent hydroxymethylation of the resulting allylic stannanes with trioxan-BF3*OEt2.

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