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6008-52-2

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6008-52-2 Usage

General Description

[1,3]DITHIEPANE is a class of organic chemical compound with a molecular formula of C4H6S2. It contains a six-membered ring consisting of four carbon atoms and two sulfur atoms, as well as a double bond between two of the carbon atoms. [1,3]DITHIEPANE is used as a building block in the synthesis of various organic molecules and pharmaceuticals due to its unique structural properties and reactivity. It is also known for its potential use in organic electronic devices and as a precursor in the production of polymers. Additionally, [1,3]DITHIEPANE has been studied for its potential applications in materials science and nanotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 6008-52-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6008-52:
(6*6)+(5*0)+(4*0)+(3*8)+(2*5)+(1*2)=72
72 % 10 = 2
So 6008-52-2 is a valid CAS Registry Number.

6008-52-2SDS

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 1,3-dithiepane

1.2 Other means of identification

Product number -
Other names 1,3-Dithiacycloheptane

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:6008-52-2 SDS

6008-52-2Downstream Products

6008-52-2Relevant articles and documents

Direct transformation of 1,3-dihalides into dithianes and dithiepines via a novel one-pot reaction with carbon disulfide and sodium borohydride

Wan, Yongqin,Kurchan, Alexei N.,Barnhurst, Loren A.,Kutateladze, Andrei G.

, p. 1133 - 1135 (2000)

1,3-Dithianes and -dithiepines are prepared via an experimentally simple and efficient direct transformation of 1,n-alkyl dihalides utilizing carbon disulfide and sodium borohydride.

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