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118525-11-4

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118525-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118525-11-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,2 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 118525-11:
(8*1)+(7*1)+(6*8)+(5*5)+(4*2)+(3*5)+(2*1)+(1*1)=114
114 % 10 = 4
So 118525-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H14BrN3/c19-14-6-8-17(9-7-14)21-22-18-12-10-16(11-13-18)20-15-4-2-1-3-5-15/h1-13,20H/b22-21+

118525-11-4SDS

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 4-[(4-bromophenyl)diazenyl]-N-phenylaniline

1.2 Other means of identification

Product number -
Other names -

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:118525-11-4 SDS

118525-11-4Downstream Products

118525-11-4Relevant articles and documents

Experimental and theoretical studies on monoazo dye including diphenylamine and N-methyldiphenylamine derivatives

Aksungur, Tu??e,Erol, Fatma,Sefero?lu, Nurgül,Sefero?lu, Zeynel

, (2020)

In this manuscript, two series of azo dyes preparing by coupling diphenylamine and N-methyl diphenylamine and diazotized substituted anilines bearing various substituents were designed and synthesized. These azo dyes were characterized by spectroscopic techniques such as 1H/13C NMR and HRMS or LCMS. Photophysical, NLO and protonation properties were investigated by experimentally and theoretically. The absorption maxima were observed in long wavelength in DMSO. The most stable tautomeric form of dyes which have tautomeric forms, were determined using model compounds. The results showed that the azo dyes are stable in azo form in all solvents used. For the usability as optic dye of the synthesized dyes, thermal property of all dyes was also determined. The all compounds are thermally stable and Td values are bigger than 220 °C.

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