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23524-64-3

23524-64-3

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23524-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23524-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,2 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23524-64:
(7*2)+(6*3)+(5*5)+(4*2)+(3*4)+(2*6)+(1*4)=93
93 % 10 = 3
So 23524-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C24H46O7S.Na/c1-3-5-7-9-11-13-15-17-19-30-23(25)21-22(32(27,28)29)24(26)31-20-18-16-14-12-10-8-6-4-2;/h22H,3-21H2,1-2H3,(H,27,28,29);/q;+1/p-1

23524-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,1,4-didecoxy-1,4-dioxobutane-2-sulfonate

1.2 Other means of identification

Product number -
Other names Butanedioic acid,2-sulfo-,1,4-didecyl ester,sodium salt (1:1)

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:23524-64-3 SDS

23524-64-3Downstream Products

23524-64-3Relevant articles and documents

Generation of quinone methide from aminomethyl(hydroxy)arenes precursors in aqueous solution

Matsumoto, Jin,Ishizu, Masayuki,Kawano, Ryu-Ichiro,Hesaka, Daisuke,Shiragami, Tsutomu,Hayashi, Yoshimi,Yamashita, Toshiaki,Yasuda, Masahide

, p. 5735 - 5740 (2005)

o-Quinone methides (QMs) are an important reactive intermediate for organic synthetic and biological standpoints of view. Photochemical and thermal transformation of N,N-dialkyl-9-aminomethyl-10-phenanthrols and their naphthalene analogs, which act as QM precursors, has been studied. These precursors readily reacted with alkyl vinyl ethers to give 2-alkoxydibenzo[f,h] chroman and 2-alkoxybenzo[f]chroman, respectively. Thermal and photochemical generation of QM was accelerated by the presence of water molecule in reaction solvents and by the formation of anionic micelle and vesicle.

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