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

78998-83-1

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78998-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78998-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,9 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78998-83:
(7*7)+(6*8)+(5*9)+(4*9)+(3*8)+(2*8)+(1*3)=221
221 % 10 = 1
So 78998-83-1 is a valid CAS Registry Number.

78998-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylsulfanylprop-2-enal

1.2 Other means of identification

Product number -
Other names 3-phenylthioprop-2-enal

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:78998-83-1 SDS

78998-83-1Relevant academic research and scientific papers

Regioselective Allylation of Enol Silyl Ethers with γ-Heterosubstituted Vinylthionium Ions.

Hunter, Roger,Michael, Joseph P.,Walter, Daryl S.

, p. 5481 - 5484 (2007/10/02)

γ-Heterosubstituted vinylthionium ions regioselectively and diastereoselectively allyate enol silyl ethers.Intramolecular capture of a vinylthionium ion is used as a key step of a novel pentannulation sequence.

SELECTIVE OXIDATION OF HYDROXY GROUPS OF PHENYLTHIO AND PHENYLSELENO ALCOHOLS

Shimizu, Makoto,Urabe, Hirokazu,Kuwajima, Isao

, p. 2183 - 2186 (2007/10/02)

Various kinds of alcohols bearing phenylthio or phenylseleno moiety were converted into the corresponding carbonyl compounds in good to excellent yields by treating with dimesityl diselenide and tert-butyl hydroperoxide.

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