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

85855-49-8

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85855-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85855-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,5 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85855-49:
(7*8)+(6*5)+(5*8)+(4*5)+(3*5)+(2*4)+(1*9)=178
178 % 10 = 8
So 85855-49-8 is a valid CAS Registry Number.

85855-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-diphenyl-1-phenylsulfanylpropan-2-one

1.2 Other means of identification

Product number -
Other names 2-Propanone,1,3-diphenyl-1-(phenylthio)

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:85855-49-8 SDS

85855-49-8Relevant academic research and scientific papers

Disulfide-based metal-free α-sulfanylation of ketones

Vaquer, Andrea F.,Frongia, Angelo,Secci, Francesco,Tuveri, Enrica

, p. 96695 - 96704 (2015/11/24)

An eco-friendly methodology for the direct α-sulfanylation of ketones, has been developed. The procedure, based on the use of functionalized diaryldisulfides and catalyzed by d,l-proline, represents a mild and efficient approach for the preparation of α-arylthio-ketones.

REGIOSPECIFIC SYNTHESIS OF α-(PHENYLTHIO)CYCLOALKENONES AND OF α-PHENYL-α-(PHENYLTHIO)KETONES VIA αα-ADDITION OF PHENYLSULPHENYL CHLORIDE TO α-DIAZOKETONES

McKervey, M. Anthony,Ratananukul, Piniti

, p. 117 - 120 (2007/10/02)

Cyclic α-diazoketones react with phenylsulphenyl chloride at room temperature to furnish α-chloro-α-(phenylthio)cycloalkanones which undergo ready dehydrochlorination to α-(phenylthio)cycloalkenones when treated with triethylamine; acyclic, terminal α-diazoketones also furnish α-chloro-α-(phenylthio)adducts which are useful electrophiles in the synthesis of α-phenyl-α-(phenylthio)ketones.

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