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

88958-78-5

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88958-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88958-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,5 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88958-78:
(7*8)+(6*8)+(5*9)+(4*5)+(3*8)+(2*7)+(1*8)=215
215 % 10 = 5
So 88958-78-5 is a valid CAS Registry Number.

88958-78-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(benzenesulfonyl)-4-methylpenta-1,3-dienyl]benzene

1.2 Other means of identification

Product number -
Other names Benzene,[[3-methyl-1-(phenylmethylene)-2-butenyl]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:88958-78-5 SDS

88958-78-5Relevant academic research and scientific papers

Integrated Chemical Process: One-Pot Double Elimination Method for Acetylenes

Orita, Akihiro,Yoshioka, Naonori,Struwe, Petra,Braier, Arnold,Beckmann, Anke,Otera, Junzo

, p. 1355 - 1363 (2007/10/03)

A novel one-pot process for synthesis of acetylenes has been achieved in which the following series of steps are integrated: addition of an α-anion of sulfone to aldehyde; trapping of the resulting adduct to incorporate a leaving group, and double elimination of this intermediate. Consolidation of Peterson elimination renders the process much simpler. This method provides a convenient and high-yielding access to a variety of enynes and polyynes as well as to functionally substituted aryl acetylenes containing halogen(s) or acetal groups, which are useful building blocks for aryl acetylene scaffolds. Iteration of the one-pot generation of acetylenic bonds provides a new metodology for the buildup of aryl acetylene skeletons.

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