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Pyridine,3,3-(1-triazene-1,3-diyl)bis-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52886-91-6

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52886-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52886-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,8 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52886-91:
(7*5)+(6*2)+(5*8)+(4*8)+(3*6)+(2*9)+(1*1)=156
156 % 10 = 6
So 52886-91-6 is a valid CAS Registry Number.

52886-91-6SDS

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 1,3-bis-(3-pyridyl)triazene

1.2 Other means of identification

Product number -
Other names 1,3-bis(3-pyridyl)triazene

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:52886-91-6 SDS

52886-91-6Relevant academic research and scientific papers

Etude du Comportement Photochimique de quelques Diaryl-1,3-triazenes

Julliard, Michel,Vernin, Gaston,Metzger, Jacques

, p. 456 - 466 (2007/10/02)

The photolysis of Diaryl-1,3-triazenes gives products whose structures are consistent with a cage recombination process of homolytically formed radicals and subsequent abstraction of hydrogen from the solvent molecules by arylamino radicals.In aromatic solvents, a free-radical chain process leads to the formation of products resulting from the homolytic substitution on the solvent.Quenching experiments show that singlet and triplet excited states are reactive but that intersystem crossing efficiency is low.

A Simmple Preparation of Aromatic or Heteroaromatic Sulphides

Giam, Choo S.,Kikukawa, Kiyoshi

, p. 756 - 757 (2007/10/02)

A simple preparation of alkyl- or aryl-thioaromatic compounds from primary aromatic and heteroaromatic amines and the appropriate disulphides has been effected using isopentyl nitrite.

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