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3326-88-3

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3326-88-3 Usage

General Description

3H-1,2-Dithiol-3-one, also known as thianthrene, is a heterocyclic compound with the molecular formula C4H2OS2. It consists of a five-membered ring containing two sulfur atoms and one oxygen atom. This chemical is known to have antibiotic properties and has been studied for its potential use in agricultural and medical applications. Additionally, 3H-1,2-Dithiol-3-one has also been investigated for its role in organic synthesis and material science. Its unique structure and properties make it an interesting subject for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 3326-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3326-88:
(6*3)+(5*3)+(4*2)+(3*6)+(2*8)+(1*8)=83
83 % 10 = 3
So 3326-88-3 is a valid CAS Registry Number.

3326-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name dithiol-3-one

1.2 Other means of identification

Product number -
Other names 1,2-Dithia-4-cyclopenten-3-on

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:3326-88-3 SDS

3326-88-3Downstream Products

3326-88-3Relevant articles and documents

HIGH-TEMPERATURE ORGANIC SYNTHESIS XLIII. REACTIONS OF ORGANIC DISELENIDES WITH PROPARGYL ALCOHOL

Deryagina, E. N.,Korchevin, N. A.,Voronkov, M. G.

, p. 1069 - 1072 (2007/10/02)

The gas-phase reaction of propargyl alcohol with dialkyl diselenides at 400 - 430 deg C leads to a high yield of 1,2-diselenol-3-one. 1,2-Diselenol-3-one is formed in a similar way from diphenyl diselenide at 450 - 500 deg C but with a low yield.The mechanism of the thermal dissociation of the diselenides and their reactions with propargyl alcohol is discussed.

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