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737758-35-9

737758-35-9

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737758-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 737758-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,7,7,5 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 737758-35:
(8*7)+(7*3)+(6*7)+(5*7)+(4*5)+(3*8)+(2*3)+(1*5)=209
209 % 10 = 9
So 737758-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H13ClO2S/c1-7(2)9-5-4-8(3)10(6-9)14(11,12)13/h4-7H,1-3H3

737758-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-5-propan-2-ylbenzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 5-Isopropyl-2-methyl-benzolsulfonylchlorid

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:737758-35-9 SDS

737758-35-9Upstream product

737758-35-9Relevant articles and documents

P-cymenesulphonyl chloride: A bio-based activating group and protecting group for greener organic synthesis

Farmer, Thomas J.,Clark, James H.,Gothe, Maite L.,Macquarrie, Duncan J.,Sherwood, James

, p. 1914 - 1919 (2015/09/22)

A bio-derived protecting/activating group has been synthesized by introducing a sulphonyl chloride group to the aromatic ring of p-cymene derived from citrus peel waste. The resulting p-cymenesulphonyl chloride was evaluated as an activating group by reacting with 1-octanol, 2-octanol, phenol and piperidine, and further reactions of the activated alcohols. The comparison to tosyl chloride demonstrates that the bio-based alternative can be effectively utilized as a direct replacement for the current fossil derived equivalent.

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