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Acetamide, N-[2-[[2-[(2-aminophenyl)azo]phenyl]azo]phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62189-02-0

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62189-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62189-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,8 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62189-02:
(7*6)+(6*2)+(5*1)+(4*8)+(3*9)+(2*0)+(1*2)=120
120 % 10 = 0
So 62189-02-0 is a valid CAS Registry Number.

62189-02-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-[[2-[(2-aminophenyl)diazenyl]phenyl]diazenyl]phenyl]acetamide

1.2 Other means of identification

Product number -
Other names Acetamide,N-[2-[[2-[(2-aminophenyl)azo]phenyl]azo]phenyl]

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:62189-02-0 SDS

62189-02-0Downstream Products

62189-02-0Relevant academic research and scientific papers

Insights into a novel class of azobenzenes incorporating 4,6- O -protected sugars as photo-responsive organogelators

Bhavya,Rabecca Jenifer,Muthuvel, Panneerselvam,Mohan Das

, p. 42219 - 42227 (2020/01/08)

A novel class of 4,6-O-butylidene/ethylidene/benzylidene β-d-glucopyranose gelator functionalized with photo-responsive azobenzene moieties were designed and synthesized and also characterized using different spectral techniques. These azobenzene-based or

Oligoazobenzenes - Switching in a new dimension

Reuter, Raphael,Hostettler, Nik,Neuburger, Markus,Wegner, Hermann A.

scheme or table, p. 180 - 183 (2011/07/07)

A new synthesis of cyclotrisazobenzene with different substituents was developed with yields of up to 30%. Solid-state structures of cyclotrisazobenzene as well as the tert-butyl derivative were obtained. Also, the photochromic properties and the complexa

Synthesis and property studies of cyclotrisazobenzenes

Reuter, Raphael,Hostettler, Nik,Neuburger, Markus,Wegner, Hermann A.

experimental part, p. 5647 - 5652 (2010/02/28)

Azobenzenophanes are fascinating macrocycles, which are of special interest due to their unique photochromic behavior. Cyclotrisazobenzenes 2 (R = H, Br, tBu) were prepared to probe how much strain the photoisomerization of the azobenzene motive can tolerate. The macrocycles were synthesized in an overall yield of 10-20% from oriho-phenylenediamine (6). Solid-state structures of cyclotrisazobenzenes 2a and 2b were obtained. Irradiation under various conditions did not induce any isomerization.

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