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(Ethylazo)- is a chemical prefix that refers to the presence of an ethylazo group in a molecule. The ethylazo group consists of an ethyl group (-CH2CH3) attached to a diazenyl group (-N=N-), forming a C2H5-N=N- structure. This functional group is often found in various organic compounds, particularly in azo dyes and pigments, where it plays a crucial role in the color properties and stability of these substances. The ethylazo group can be introduced into a molecule through chemical reactions, such as coupling reactions involving diazonium salts and phenols or amines. Overall, the (ethylazo)- prefix is an essential component in the synthesis and characterization of a wide range of organic compounds, particularly those with significant color and stability attributes.

935-08-0

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935-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 935-08-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 935-08:
(5*9)+(4*3)+(3*5)+(2*0)+(1*8)=80
80 % 10 = 0
So 935-08-0 is a valid CAS Registry Number.

935-08-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethylphenyl diimide

1.2 Other means of identification

Product number -
Other names Aethyl-phenyl-diazen

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:935-08-0 SDS

935-08-0Relevant academic research and scientific papers

Aryl Pyrazoles from Photocatalytic Cycloadditions of Arenediazonium

Cardinale, Luana,Neumeier, Michael,Majek, Michal,Jacobi Von Wangelin, Axel

, p. 7219 - 7224 (2020/10/02)

A photocatalytic synthesis of 1,5-diaryl pyrazoles from arenediazoniums and arylcyclopropanols is reported. The reaction proceeded under mild conditions (rt, 20 min) with catalytic [Ru(bpy)3]2+ under blue-light irradiation and exhibited compatibility with several functional groups (e.g., I, SF5, SO2NH2, N3, CN) and perfect levels of regiocontrol. Mechanistic studies (luminescence spectroscopy, CV, DFT, radical trapping, quantum yield determination) documented an initial oxidative quenching of the excited photocatalyst and the operation of a radical-chain mechanism.

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