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29418-48-2

29418-48-2

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29418-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29418-48-2 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 29418-48:
(7*2)+(6*9)+(5*4)+(4*1)+(3*8)+(2*4)+(1*8)=132
132 % 10 = 2
So 29418-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H14N2O2/c1-17-12-9-6-10-13(18-2)14(12)16-15-11-7-4-3-5-8-11/h3-10H,1-2H3/b16-15+

29418-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,6-dimethoxyphenyl)-phenyldiazene

1.2 Other means of identification

Product number -
Other names 2,6-Dimethoxyazobenzol

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:29418-48-2 SDS

29418-48-2Downstream Products

29418-48-2Relevant articles and documents

Calculated oxidation potentials predict reactivity in Baeyer-Mills reactions

Gingrich, Phillip W.,Olson, David E.,Tantillo, Dean J.,Tombari, Robert J.,Tuck, Jeremy R.,Yardeny, Noah

supporting information, p. 7575 - 7580 (2021/09/22)

Azobenzenes are widely used as dyes and photochromic compounds, with the Baeyer-Mills reaction serving as the most common method for their preparation. This transformation is often plagued by low yields due to the formation of undesired azoxybenzene. Here, we explore electronic effects dictating the formation of the azoxybenzene side-product. Using calculated oxidation potentials, we were able to predict reaction outcomes and improve reaction efficiency simply by modulating the oxidation potential of the arylamine component.

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