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90633-60-6

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90633-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90633-60-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,3 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90633-60:
(7*9)+(6*0)+(5*6)+(4*3)+(3*3)+(2*6)+(1*0)=126
126 % 10 = 6
So 90633-60-6 is a valid CAS Registry Number.

90633-60-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hex-2-enylsulfonyl-4-methylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,1-(2-hexenylsulfonyl)-4-methyl

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:90633-60-6 SDS

90633-60-6Downstream Products

90633-60-6Relevant articles and documents

Regio- and Stereoselective Synthesis of (E)- and (Z)-Vinylic Sulfones and Their Conversion to the Corresponding Allylic Sulfones

Kobayashi, Toshifumi,Tanaka, Yuhji,Ohtani, Takashi,Kinoshita, Hideki,Inomata, Katsuhiko,Kotake, Hiroshi

, p. 1209 - 1212 (2007/10/02)

(E)- and (Z)-vinilyc sulfones were prepared regio- and stereoselectively from 1-alkenes or 1-alkynes in high yields via iodosulfonization in AcOEt-H2O.The vinylic sulfones thus prepared were converted to the corresponding allylic sulfones by treatment wit

A CONVENIENT METHOD FOR THE PREPARATION OF α-ALKYLATED VINYLIC SULFONES AND THEIR CONVERSION TO ALLYLIC SULFONES

Inomata, Katsuhiko,Tanaka, Yuhji,Sasaoka, Shin-ichi,Kinoshita, Hideki,Kotake, Hiroshi

, p. 341 - 344 (2007/10/02)

2-Pyrrolidinoalkyl p-tolyl sulfones, which were readily available by the addition of pyrrolidine to vinylic or allylic sulfones, were converted to the corresponding α-alkylated vinylic sulfones through α-alkylation followed by elimination of pyrrolidino g

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