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1-Propanone, 3-[(1,1-dimethylethyl)thio]-1,3-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21205-13-0

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21205-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21205-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,0 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21205-13:
(7*2)+(6*1)+(5*2)+(4*0)+(3*5)+(2*1)+(1*3)=50
50 % 10 = 0
So 21205-13-0 is a valid CAS Registry Number.

21205-13-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-tert-butylsulfanyl-1,3-diphenylpropan-1-one

1.2 Other means of identification

Product number -
Other names 3-tert-Butylmercapto-1,3-diphenyl-propan-1-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:21205-13-0 SDS

21205-13-0Downstream Products

21205-13-0Relevant academic research and scientific papers

Scope and limitations of HClO4-SiO2 as an extremely efficient, inexpensive, and reusable catalyst for chemoselective carbon-sulfur bond formation

Khatik, Gopal L.,Sharma, Gaurav,Kumar, Raj,Chakraborti, Asit K.

, p. 1200 - 1210 (2007)

The scope and limitations of perchloric acid adsorbed on silica gel (HClO4-SiO2) as a highly efficient, inexpensive, and reusable catalyst for chemoselective carbon-sulfur bond formation by conjugate addition of thiols to α,β-unsatur

Sc(III)-catalyzed enantioselective addition of thiols to α,β-unsaturated ketones in neutral water

Bonollo, Simona,Lanari, Daniela,Pizzo, Ferdinando,Vaccaro, Luigi

supporting information; body text, p. 2150 - 2152 (2011/06/21)

Chemical equations presented. This report concerns Lewis acid catalyzed enantioselective sulfa-Michael addition in neutral water by using a very efficient Sc(OTf)3/bipyridine 1 catalytic system. It is noteworthy that the protocol presented empl

A bifunctional cinchona alkaloid-squaramide catalyst for the highly enantioselective conjugate addition of thiols to transchalcones

Dai, Le,Wang, Su-Xi,Chen, Fen-Er

supporting information; experimental part, p. 2137 - 2141 (2010/11/05)

A chiral squaramide catalysts-promoted asymmetric sulfa-Michael conjugated addition of thiols to trans-chalcones is presented. Moderate to excellent yields and high enantioselectivities (up to 99% ee) were achieved under mild conditions.

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