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80028-57-5

80028-57-5

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80028-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80028-57-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,2 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80028-57:
(7*8)+(6*0)+(5*0)+(4*2)+(3*8)+(2*5)+(1*7)=105
105 % 10 = 5
So 80028-57-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H8S2/c1-2-6-7-4-3-5-8-6/h2-4,6H,1,5H2

80028-57-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethenyl-4H-1,3-dithiine

1.2 Other means of identification

Product number -
Other names 2-Ethenyl-4H-1,3-dithiin

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:80028-57-5 SDS

80028-57-5Downstream Products

80028-57-5Relevant articles and documents

(E,Z)-Ajoene: A potent antithrombotic agent from garlic

Block,Ahmad,Jain,et al.

, p. 8295 - 8296 (2007/10/02)

A report is presented of the structural characterization and simple synthesis of (E,Z)-ajoene.

Gas Phase Reactions, 30. Thioacrolein: The Most Stable Isomer C3H4S and its PE Spectroscopic Proof in the Gas Phase

Bock, Hans,Mohmand, Shamsher,Hirabayashi, Takakuni,Semkow, Andrzej

, p. 1339 - 1348 (2007/10/02)

The ensemble C3H4S contains 13 valence-"normal" isomers, of which according to MNDO calculations thioacrolein, H2C=C(H)-C(H)=S, should be the energetically most stable.Expectedly, diallyl sulfide decomposes on pyrolysis at 660 K to yield propene and thioacrolein, which can be cool-trapped in a preparative way as mixture of Diels-Alder dimers.Heating of the isomeric dimeres leads in a retrodiene splitting to pure thioacrolein, identified by its PE spectrum which is similar to that of acrolein.

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