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2-Methyl-2-methylthio-1-phenyl-1-propanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54394-72-8

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54394-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54394-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,9 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54394-72:
(7*5)+(6*4)+(5*3)+(4*9)+(3*4)+(2*7)+(1*2)=138
138 % 10 = 8
So 54394-72-8 is a valid CAS Registry Number.

54394-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-methylthio-1-phenyl-1-propanone

1.2 Other means of identification

Product number -
Other names 2-methyl-2-(methylthio)propiophenone

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:54394-72-8 SDS

54394-72-8Relevant academic research and scientific papers

Rhodium-catalyzed phenylthiolation reaction of heteroaromatic compounds using α-(phenylthio)isobutyrophenone

Arisawa, Mieko,Toriyama, Fumihiko,Yamaguchi, Masahiko

supporting information; experimental part, p. 2344 - 2347 (2011/05/16)

In the presence of catalytic amounts of RhH(PPh3)4 and 1,2-bis(diphenylphosphino)ethane (dppe), 1,3-benzothiazoles, 1,3-benzoxazoles, and benzothiophene reacted with α-(phenylthio) isobutyrophenone giving 2-phenylthio derivatives. Reactive monocyclic heteroaromatics, 1-methyl-1,2,3,4-tetrazole and 2-cyanothiophene were also converted into the 5-phenylthio derivatives. The use of an appropriate phenylthio transfer reagent is crucial for the efficient catalyzed conversion of heteroaromatic C-H bonds into C-S bonds.

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