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5071-69-2

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5071-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5071-69-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,7 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5071-69:
(6*5)+(5*0)+(4*7)+(3*1)+(2*6)+(1*9)=82
82 % 10 = 2
So 5071-69-2 is a valid CAS Registry Number.

5071-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-[(4-bromophenyl)methylidene]-1-cyclohexyl-2-methyl-5-oxopyrrole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 1,1-Dichlor-penta-1,4-dien-4-carbonsaeure-methylester

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:5071-69-2 SDS

5071-69-2Downstream Products

5071-69-2Relevant articles and documents

Decomposition and Isomerization of Bridgehead Cis 1,2-Diazenes (Azoalkanes)

Chae, Woo-Ki,Baughman, Sharon A.,Engel, Paul S.,Bruch, Manfred,Oezmeral, Cenan,et al.

, p. 4824 - 4833 (2007/10/02)

Four acyclic cis 1,2-diazenes, azo-1-adamantane (cis-ada), azo-bicyclooctane (cis-), azo-1-bicycloheptane (cis-), and azo-1-bicyclohexane (cis-) have been generated by UV irradiation of the corresponding trans-isomers.These compounds differ greately in stability, cis- easily surviving at 100 deg C and cis-ada not being isolable.Whereas cis- and cis-only isomerize back to trans on heating, the other two compounds undergo competing loss of nitrogen.The observation that the energy of the transition state for isomerization remains at 42 +/- 1 kcal mol-1 regardless of the cis ground state energy is used to argue that thermal isomerization proceeds via semilinearization rather than rotation.A remarkable correlation of cis ground state energy with cis n,?* excitation energy has emerged from this study.

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