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83650-24-2

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83650-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83650-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,5 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83650-24:
(7*8)+(6*3)+(5*6)+(4*5)+(3*0)+(2*2)+(1*4)=132
132 % 10 = 2
So 83650-24-2 is a valid CAS Registry Number.

83650-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dicarbomethoxy-3,6-dimethoxy-1,4-cyclohexa-1,4-diene

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:83650-24-2 SDS

83650-24-2Relevant articles and documents

1,4-dimethoxy-1,3-butadiene as a Donor Diene in Diels-Alder Cycloadditions

Hiranuma Hidetoshi,Miller, Sidney I.

, p. 5083 - 5088 (2007/10/02)

The title compound (DMBU) is a useful diene in cycloadditions.Since DMBU is readily obtained in two steps from 1,4-dihydroxy-2-butyne, it should be regarded as an inexpensive and abundant starting material.Diels Alder products were obtained from DMBU and the dienophiles, dimethyl acetylenedicarboxylate, ethyl propiolate, benzyne, fumaronitrile, tetracyanoethene, maleic anhydride, 1,2-dibenzoylethene, diethyl azodicarboxylate, and four 1,4-quinones.The aromatization of some of these products was studied.As determined by gas chromatography and 1H NMR, DMBU is obtained as three isomers Z,Z/Z,E/E,E = (60 +/-3):(34 +/- 3):(6 +/- 2).While the Z,Z form is less reactive, the Z,E and E,E isomers react with tetracyanoethene at rates similar to that of 1-methoxy-1,3-butadiene.

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