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

78998-90-0

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78998-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78998-90-0 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, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78998-90:
(7*7)+(6*8)+(5*9)+(4*9)+(3*8)+(2*9)+(1*0)=220
220 % 10 = 0
So 78998-90-0 is a valid CAS Registry Number.

78998-90-0SDS

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-phenylselanylprop-2-en-1-ol

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:78998-90-0 SDS

78998-90-0Relevant academic research and scientific papers

Diphenyl diselenide-promoted radical addition of benzeneselenol to acetylenes

Ogawa,Obayashi,Sekiguchi,Masawaki,Kambe,Sonoda

, p. 1329 - 1332 (2007/10/02)

Diphenyl diselenide promotes the radical addition of benzeneselenol to inactivated acetylenes upon irradiation through Pyrex with a tungsten lamp. The addition may proceed by a radical chain mechanism that involves phenylseleno radical (PhSe·) as the key

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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