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(E)-1-(2-methoxyphenyl)-2-(4-methylphenyl)diazene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29418-41-5

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29418-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29418-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,1 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29418-41:
(7*2)+(6*9)+(5*4)+(4*1)+(3*8)+(2*4)+(1*1)=125
125 % 10 = 5
So 29418-41-5 is a valid CAS Registry Number.

29418-41-5SDS

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 (2-methoxyphenyl)-(4-methylphenyl)diazene

1.2 Other means of identification

Product number -
Other names 2-METHOXY-4'-METHYLAZOBENZENE

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:29418-41-5 SDS

29418-41-5Relevant academic research and scientific papers

Aryliminodimagnesium Reagents. XIV. Reactions with Nitrobenzenes Having Electronegative ortho-Substituents. Effects of Reaction Conditions on Condensation, Replacement, and Substitution

Okubo, Masao,Inatomi, Yoshito,Taniguchi, Naoki,Imamura, Kaori

, p. 3581 - 3586 (2007/10/02)

In reactions of ArN(MgBr)2 with o-MeO- and o-halo-substituted nitrobenzenes, types and yields of products were different from those in its reactions with m- and p-substituted substrates.Condensation (leading to unsymmetrical azoxy- and azobenzenes), o-substituent replacement, and nuclear substitution took place.Relative yields of products were greatly affected by substituents and reaction conditions. o-MeO and o-F favor replacement, while o-Cl, o-Br, and o-I favor substitution.Replacement and/or substitution predominate when small molar excess of reagent and low concentration are used, while condensation predominates when large molar excess of reagent and high concentration are used, which phenomenon is mechanistically discussed.

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