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3-Buten-2-one, 1,1,1-trifluoro-4,4-bis(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

673448-46-9

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673448-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 673448-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,3,4,4 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 673448-46:
(8*6)+(7*7)+(6*3)+(5*4)+(4*4)+(3*8)+(2*4)+(1*6)=189
189 % 10 = 9
So 673448-46-9 is a valid CAS Registry Number.

673448-46-9SDS

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 β-trifluoroacetylketene diphenyldithioacetal tetroxide

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:673448-46-9 SDS

673448-46-9Relevant academic research and scientific papers

A novel effective electrophile: β-trifluoroacetylketene diphenyldithioacetal S,S-tetroxide

Krasovsky, Arkady L.,Druzhinin, Sergej V.,Nenajdenko, Valentine G.,Balenkova, Elizabeth S.

, p. 1129 - 1132 (2007/10/03)

A synthesis of a novel electrophilic reagent - β- trifluoroacetylketene diphenyldithioacetal S,S-tetroxide 3 is described. The reaction of 3 with various electron-rich aromatics such as 1,3-dimethoxybenzene, 2-methylthiophene, N-methylpyrrole, and 2-methylindole was investigated. In the course of these reactions an unusual migration of a phenylsulfonyl group takes place. An easy and ready for scale-up procedure for the synthesis of previously unknown β-aryl, α-phenylsulphonyl substituted α,β-unsaturated trifluoromethyl ketones is reported.

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