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70332-97-7

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70332-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70332-97-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,3 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70332-97:
(7*7)+(6*0)+(5*3)+(4*3)+(3*2)+(2*9)+(1*7)=107
107 % 10 = 7
So 70332-97-7 is a valid CAS Registry Number.

70332-97-7SDS

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 1,4-Cyclohexadien-1,2-dicarbonsaeure-di-tert-butylester

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:70332-97-7 SDS

70332-97-7Relevant articles and documents

Alkynes and Cumulenes, XII. The Application of Di-tert-butyl Acetylenedicarboxylate in Diels-Alder Additions

Weber, Gisela,Menke, Klaus,Hopf, Henning

, p. 531 - 541 (2007/10/02)

Di-tert-butyl acetylenedicarboxylate (1) may be added in good yields to the model dienes 1,3-butadiene (6a), 2-methyl-1,3-butadiene (6b), 2,3-dimethyl-1,3-butadiene (6c), furan (10), and 1,3-cyclohexadiene (19) to afford the Diels-Alder adducts 7a-c, 12 (E = CO2C(CH3)3), and 20, respectively.Under certain conditions the reaction with 10 also laeds to the four 2:1-adducts 13-16 (E = CO2C(CH3)3).Whereas the esters 7a-c are converted in quantitative yields to the corresponding anhydrides 8a-c by warming in the presence of catalytic amounts of p-toluenesulfonic acid or by heating in substance, the decomposition of 12 and 20 stops at the stage of the monoesters 17 and 21, respectively.Competition experiments show that 1 is approximately three times less reactive towards 6c than dimethyl acetylenedicarboxylate (11).It is shown that 1 is a useful dienophile for the preparation of "mixed" paracyclophanes of type 28.

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