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(4-azidobut-1-yne-1,4-diyl)dibenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

915696-34-3

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915696-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 915696-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,6,9 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 915696-34:
(8*9)+(7*1)+(6*5)+(5*6)+(4*9)+(3*6)+(2*3)+(1*4)=203
203 % 10 = 3
So 915696-34-3 is a valid CAS Registry Number.

915696-34-3SDS

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 (4-azidobut-1-yne-1,4-diyl)dibenzene

1.2 Other means of identification

Product number -
Other names 4-azido-1,4-diphenylbutyne

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:915696-34-3 SDS

915696-34-3Upstream product

915696-34-3Downstream Products

915696-34-3Relevant academic research and scientific papers

Cyclization reactions of homopropargyl azide derivatives catalyzed by PtCl4 in ethanol solution: Synthesis of functionalized pyrrole derivatives

Hiroya, Kou,Matsumoto, Shigemitsu,Ashikawa, Masayasu,Ogiwara, Kentaro,Sakamoto, Takao

, p. 5349 - 5352 (2006)

PtCl4-catalyzed cyclization reactions of homopropargyl azide derivatives to pyrrole rings were investigated. Using ethanol as solvent with 2,6-di-tert-butyl-4-methylpyridine as the base was found to be the best set of conditions for effecting this ring-closing reaction. These reaction conditions can be applied to the preparation of functionalized pyrrole derivatives, with no effect on the functional groups.

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