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13666-95-0

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13666-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13666-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,6 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13666-95:
(7*1)+(6*3)+(5*6)+(4*6)+(3*6)+(2*9)+(1*5)=120
120 % 10 = 0
So 13666-95-0 is a valid CAS Registry Number.

13666-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names Acetamide,N,N'-(azodi-2,1-phenylene)bis

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:13666-95-0 SDS

13666-95-0Relevant articles and documents

Synthesis and photochemical properties of oligo-ortho-azobenzenes

Bellotto, Silvia,Reuter, Raphael,Heinis, Christian,Wegner, Hermann A.

, p. 9826 - 9834 (2012/01/06)

Azobenzenes have attracted great interest in recent years because of their ability to change conformation upon irradiation. This property has been featured in several applications not only in organic chemistry but also in biology. Even though monoazobenzenes have been extensively studied and documented in the literature, only a few methods are available for the synthesis of oligo-ortho-azobenzenes. Also, their photochemical properties have not been reported so far. This study shows an efficient strategy for the preparation of oligo-ortho-azobenzenes and the investigation of their photochemical properties. It is demonstrated that the absorption spectra are highly influenced by the substituents. Interestingly, none of the ortho-bis-, tris-, or tetra-azobenzenes showed any E → Z isomerization. Only the ortho-nitrogen-substituted monoazobenzenes' photochromic behavior upon UV irradiation was observed.

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