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

88626-34-0

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88626-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88626-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,6,2 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88626-34:
(7*8)+(6*8)+(5*6)+(4*2)+(3*6)+(2*3)+(1*4)=170
170 % 10 = 0
So 88626-34-0 is a valid CAS Registry Number.

88626-34-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [((2E,4E)-Nona-2,4-diene)-2-sulfonyl]-benzene

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:88626-34-0 SDS

88626-34-0Downstream Products

88626-34-0Relevant academic research and scientific papers

SYNTHESES WITH SULFONES XLV: STEREOSELECTIVE PREPARATION OF 1- BENZENESULFONYL-1,3-DIENES

Cuvigny, T.,Penhoat, C. Herve du,Julia, M.

, p. 5321 - 5328 (2007/10/02)

The stereoselective preparation of EE 1-benzenesulfonyl-1,3-dienes is described.Michael addition and Diels-Alder cycloaddition of these compounds are reported.

Synthesis with Sulfones (n0XXX) : Stereoselective Synthesis of Arenesulfonyl-1,3-dienes.

Cuvigny, T.,Penhoat, C. Herve du,Julia, M.

, p. 4315 - 4318 (2007/10/02)

Basic treatment of allylic 1,1-disulfones gives 1-arenesulfonyl 1,3-dienes.Condensation of aldehydes with lithiated allylic sulfones and in situ acetylation of the alkoxide thus formed followed by basic elimination of acetic acid leads to EE 2-arenesulfon

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