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4-({4-nitro-1-naphthyl}diazenyl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83733-42-0

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83733-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83733-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,3 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83733-42:
(7*8)+(6*3)+(5*7)+(4*3)+(3*3)+(2*4)+(1*2)=140
140 % 10 = 0
So 83733-42-0 is a valid CAS Registry Number.

83733-42-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-(4-hydroxyphenylazo)-4-nitronaphthalene

1.2 Other means of identification

Product number -
Other names (4-Nitro-naphthalin)-(1 azo 4)-phenol

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:83733-42-0 SDS

83733-42-0Relevant academic research and scientific papers

N,N'-Disubstituted Naphthyl(Azo)-2,3-Dihydroperimidine Blue Dyes Exhibiting High Solubility in Ferroelectric Liquid Crystal Hosts

O'Brien, M. K.,Shannon, P. J.,Grasso, R. P.

, p. 167 - 175 (2007/10/02)

The synthesis of N,N'-disubstituted naphthyl(azo)-2,3-dihydroperimidine blue dyes and a comparison of their absorption maxima and solubility in ferroelectric liguid crystal (FLC) hosts is described.The N,N'-disubstituted azo perimidines exhibited a much h

Cyclometalation of Arylazo Compounds. Part 2. Regioselectivity of the Cyclopalladation of Some Substituted 1-Arylazonaphthalenes

Hugentobler, Max,Klaus, Alfred J.,Mettler, Hanspeter,Rys, Paul,Wehrle, Gabi

, p. 1202 - 1211 (2007/10/02)

A variety of cyclopalladated 1-arylazonaphthalenes is described, where ortho-palladation occurs at C(2) in the naphthyl ring or at C(2' or 6') in the phenyl moiety.Two examples of peri-cyclopalladation at C(8) in the naphthyl ring are presented.The electronic and steric influences of substituents at either arene moiety on the relative basicities of the azo-N-atoms and the relative nucleophilicities of the potential palladation sites C(2), C(2' or 6'), and C(8) are discussed qualitatively in order to rationalize the observed regioselectivity.

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