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13003-40-2

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13003-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13003-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,0 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13003-40:
(7*1)+(6*3)+(5*0)+(4*0)+(3*3)+(2*4)+(1*0)=42
42 % 10 = 2
So 13003-40-2 is a valid CAS Registry Number.

13003-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2-tetrakis(trifluoromethylsulfanyl)ethene

1.2 Other means of identification

Product number -
Other names Tetrakis-trifluormethyl-mercapto-ethylen

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:13003-40-2 SDS

13003-40-2Downstream Products

13003-40-2Relevant articles and documents

Preparation of Perfluorinated Hexakis(alkylthio- and -seleno)ethanes

Schlosser, Karl

, p. 1083 - 1088 (2007/10/02)

The perfluorinated perhetero-substituted ethanes 2a - c are prepared by irradiation of the thiocarbonates 1a - c.Upon UV-irradiation (λmax = 300 nm) bis(trifluoromethyl) trithiocarbonate (1a) decomposes by a cage process to give carbon disulfide, trifluoromethyl- and trifluoromethylthiyl radicals.In the solvent cage these radicals partly dimerize producing 3.The formation of 2a is interpreted in terms of a competition between this combination process and trapping of trifluoromethyl radicals by 1a, forming 4a, which then dimerizes.A similar mechanistic pathway is pro posed for the formation of 2b and 2c.

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