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5222-76-4

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5222-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5222-76-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,2 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5222-76:
(6*5)+(5*2)+(4*2)+(3*2)+(2*7)+(1*6)=74
74 % 10 = 4
So 5222-76-4 is a valid CAS Registry Number.

5222-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-1,3-hexadien-5-yne

1.2 Other means of identification

Product number -
Other names cis-1,3-Hexadien-5-in

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:5222-76-4 SDS

5222-76-4Upstream product

5222-76-4Relevant articles and documents

Shock Tube Study of Thermal Rearrangement of 1,5-Hexadiyne over Wide Temperature and Pressure Regime

Tranter, Robert S.,Tang, Weiyong,Anderson, Ken B.,Brezinsky, Kenneth

, p. 3406 - 3415 (2004)

The pyrolysis of 1,5-hexadiyne has been studied in a high-pressure single pulse shock tube to investigate the mechanisms involved in the production of benzene from propargyl radicals. Analysis of the reaction products by gas chromatography and matrix isolation Fourier transform infrared spectroscopy has positively identified six linear C6H6 species and two cyclic C6H6 species. Of these species cis-1,3-hexadien-5- yne and trans-1,3-hexadiene-5-yne have been unambiguously identified for the first time and provide vital information concerning a low-temperature route to benzene that does not involve the formation of fulvene; however, the data also provide support for two high-temperature paths from propargyl radicals to benzene via fulvene. Thus experimental evidence has been gained that supports two different routes to benzene formation. The mechanisms and rate coefficients that have been obtained in this work are discussed.

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