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52072-12-5

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52072-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52072-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,7 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52072-12:
(7*5)+(6*2)+(5*0)+(4*7)+(3*2)+(2*1)+(1*2)=85
85 % 10 = 5
So 52072-12-5 is a valid CAS Registry Number.

52072-12-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name α-acetoxyallyl phenyl sulfide

1.2 Other means of identification

Product number -
Other names 1-(Phenylthio)-prop-2-enylacetat

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:52072-12-5 SDS

52072-12-5Downstream Products

52072-12-5Relevant articles and documents

Direct α-acyloxylation of organic sulfides with the hypervalent (diacyloxyiodo)benzene/tetra-n-butylammonium bromide (TBAB) reagent combination

Zhu, Dan,Chang, Denghu,Gan, Shaoyan,Shi, Lei

, p. 27983 - 27987 (2016/04/04)

A novel metal-free approach to directly synthesize α-acyloxy sulfides from readily available alkyl sulfides utilizing the hypervalent (diacyloxyiodo)benzene and TBAB reagent combination is reported. This transformation is characterized by its broad substrate scope in moderate to excellent yields, convenient operating conditions and outstanding functional group tolerance.

CONVERSIONS OF ALLYL ARYL SULFOXIDES UNDER PUMMERER REARRANGEMENT CONDITIONS

Fedorov, N. V.,Shevchenko, M. V.,Anisimov, A. V.,Viktorova, E. A.

, p. 624 - 626 (2007/10/02)

In the presence of acetic acid, allyl phenyl sulfoxides forms α-acetoxyallyl phenyl sulfides and 2-acetoxymethyl-2,3-dihydrobenzothiophene; under the same conditions allyl 1-naphthyl sulfoxide gives 2-methyl-2,3-dihydronaphtho-thiophenoxide.

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