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4-(4-Chlorophenylazo)-1-naphtylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42950-00-5

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42950-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42950-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,5 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 42950-00:
(7*4)+(6*2)+(5*9)+(4*5)+(3*0)+(2*0)+(1*0)=105
105 % 10 = 5
So 42950-00-5 is a valid CAS Registry Number.

42950-00-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-chloro-phenylazo)-[1]naphthylamine

1.2 Other means of identification

Product number -
Other names 4-<4-Chlorphenylazo>-1-naphthylamin

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:42950-00-5 SDS

42950-00-5Relevant academic research and scientific papers

Effects of different terminal substituents on the mesomorphic behavior of some azo-Schiff base and azo-ester-based liquid crystals

Thaker,Kanojiya,Tandel

scheme or table, p. 120 - 137 (2011/05/12)

In order to investigate the influence of the terminal substitution on mesomorphism, two new series of azo-Schiff base and azo-ester liquid crystals having the following structures have been synthesized. All the compounds possess mesomorphic properties. In series A compounds A1 and A3 exhibit only a nematic mesophase, whereas compounds A2, A4, A5, A6, A7, A8, A9, and A10 exhibit a smectic as well as a nematic phase. In series B compounds B1 to B9 exhibit only a nematic mesophase, and compounds B10 and B11 exhibit a smectic as well as a nematic phase, but compound B12 exhibits only a smectic phase. All these compounds were characterized by elemental analyses and spectroscopic techniques (Fourier transform infrared [FTIR], 1H nuclear magnetic resonance [NMR], and mass spectroscopy). Their mesomorphic properties were measured by optical polarized light microscopy and differential scanning calorimetry (DSC). Copyright Taylor & Francis Group, LLC.

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