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Benzene, (1-octenylseleno)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60466-44-6

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60466-44-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60466-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,6 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60466-44:
(7*6)+(6*0)+(5*4)+(4*6)+(3*6)+(2*4)+(1*4)=116
116 % 10 = 6
So 60466-44-6 is a valid CAS Registry Number.

60466-44-6SDS

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 [(1E)-oct-1-en-1-ylseleno]benzene

1.2 Other means of identification

Product number -
Other names [((E)-Oct-1-enyl)selanyl]-benzene

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:60466-44-6 SDS

60466-44-6Relevant academic research and scientific papers

Highly regioselective hydroselenation of inactivated terminal alkynes using diselenide-Ph2P(O)H mixed systems under visible-light irradiation

Kobiki, Yohsuke,Kawaguchi, Shin-Ichi,Ogawa, Akiya

, p. 5453 - 5456 (2013/09/23)

Upon visible-light irradiation, we could achieve a highly regioselective hydroselenation of inactivated terminal alkynes to give 1-(organylseleno)-1- alkenes by using diselenide-Ph2P(O)H mixed systems. The photoinduced hydroselenation presented in this study is advantageous as it does not involve the handling of oxygen-sensitive and foul-smelling selenols.

Preparation of (Z)- and (E)-vinyl selenides utilizing vinylboronic acids and vinylboronic esters in ionic liquids

Kabalka, George W.,Venkataiah, Bollu

, p. 3703 - 3705 (2007/10/03)

Vinylboronic acids and vinylboronic esters react with phenylselenyl chloride in ionic liquids to generate vinyl selenides stereospecifically.

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