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[(1-Cyclohexenyl)azo]benzene, also known as 1-(phenylazo)cyclohexene, is an organic compound with the chemical formula C12H14N2. It is a derivative of azobenzene, featuring a cyclohexene ring attached to the azo group. This yellow crystalline solid is characterized by its UV-Vis absorption properties, making it potentially useful in applications such as dyes, pigments, and photochemical studies. The compound is synthesized by coupling a cyclohexenyl compound with a diazonium salt, and its structure and properties are of interest in the field of organic chemistry, particularly in the study of azo compounds and their applications.

5300-19-6

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5300-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5300-19-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,0 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5300-19:
(6*5)+(5*3)+(4*0)+(3*0)+(2*1)+(1*9)=56
56 % 10 = 6
So 5300-19-6 is a valid CAS Registry Number.

5300-19-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenylazocyclohex-1-ene

1.2 Other means of identification

Product number -
Other names 1-Phenylazo-cyclohex-1-en

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 -
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More Details:5300-19-6 SDS

5300-19-6Relevant academic research and scientific papers

Applications of Azoalkenes in the Synthesis of Fused Ring Pyridazine Derivatives

Gaonkar, Santosh L.,Lokanatha Rai

, p. 1346 - 1348 (2015/10/06)

Cyclic ketohydrazones containing α-methylene group are oxidized by chloramine-T followed by treatment with triethylamine leads to the formation of azoalkenes via azochloride, which are trapped by olefinic compounds to produce fused ring pyridazine derivatives in good yield.

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