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

74824-70-7

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74824-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74824-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,2 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74824-70:
(7*7)+(6*4)+(5*8)+(4*2)+(3*4)+(2*7)+(1*0)=147
147 % 10 = 7
So 74824-70-7 is a valid CAS Registry Number.

74824-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylselanylprop-2-enal

1.2 Other means of identification

Product number -
Other names -

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:74824-70-7 SDS

74824-70-7Relevant academic research and scientific papers

Selenium in Organic Synthesis: A Novel Route to 1-Phenylselenobutadienes and 1,4-Dicarbonyl Compounds

Comasseto, J. V.,Brandt, C. A.

, p. 146 - 149 (2007/10/02)

Two approaches to 1-phenylseleno-1,3-butadienes 5 are reported, via phenylselenoalkenylidene phosphoranes and phenylselenoalkenals, respectively. 1,4-Dicarbonyl compounds are prepared from the 1-phenylselenobutadienes or from the phenylselenoalkenals.

Oxidation of Alcohols with tert-Butyl Hydroperoxide and Diaryl Diselenide

Kuwajima, Isao,Shimizu, Makoto,Urabe, Hirokazu

, p. 837 - 842 (2007/10/02)

Treatment of alcohols with tert-butyl hydroperoxide in the presence of diaryl diselenide in refluxing benzene gives the corresponding aldehydes or ketones.Although some allylic alcohols undergo oxidation in the presence of 10-15 mol percent of bis(p-chlorophenyl) diselenide, use of 0.5 equiv of bis(2,4,6-trimethylphenyl) diselenide gives satisfactory results in almost all cases.The procedure can be used for selective oxidation of alcohols bearing a phenylthio or phenylseleno group, which usually survives the reaction conditions to give the corresponding carbonyl compounds.

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