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38382-55-7

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38382-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38382-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,8 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38382-55:
(7*3)+(6*8)+(5*3)+(4*8)+(3*2)+(2*5)+(1*5)=137
137 % 10 = 7
So 38382-55-7 is a valid CAS Registry Number.

38382-55-7SDS

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 6-methylene-2,4-cyclohexadienylideneketene

1.2 Other means of identification

Product number -
Other names -

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:38382-55-7 SDS

38382-55-7Upstream product

38382-55-7Relevant articles and documents

Generation of 6-methylene-2,4-cyclohexadienylideneketene by flash photolysis of benzocyclobutenone in aqueous solution and study of the reactions of this ketene in that medium

Chiang,Kresge,Zhan

, p. 607 - 611 (2003)

Flash photolysis of benzocyclobutenone in aqueous solution produced a transient species with a microsecond lifetime whose rates of decay were measured in perchloric acid, sodium hydroxide, and buffer solutions over the acidity range [H+] 1 × 10-13 - 100 M. This produced a rate profile, isotope effects, and buffer behaviour typical of ketene reactions, and that, together with product identification, served to identify this transient as 6-methylene-2,4-cyclohexadienylideneketene, formed by electrocyclic opening of the four-membered ring of benzocyclobutenone. Comparison of rates of reaction of this ketene with those of its saturated analog, pentamethyleneketene, produced some expected as well as some unexpected results.

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