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84065-55-4

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84065-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84065-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,6 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84065-55:
(7*8)+(6*4)+(5*0)+(4*6)+(3*5)+(2*5)+(1*5)=134
134 % 10 = 4
So 84065-55-4 is a valid CAS Registry Number.

84065-55-4SDS

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 phenylselanyl radical

1.2 Other means of identification

Product number -
Other names phenylselenyl radical

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:84065-55-4 SDS

84065-55-4Upstream product

84065-55-4Relevant academic research and scientific papers

Thermochemistry of arylselanyl radicals and the pertinent ions in acetonitrile

Holm, Allan Hjarbaek,Yusta, Laura,Carlqvist, Peter,Brinck, Tore,Daasbjerg, Kim

, p. 2148 - 2157 (2003)

Reduction and oxidation potentials of a series of parasubstituted phenylselanyl radicals, XC6H4Se., have been measured using photomodulated voltammetry in acetonitrile. The thermodynamic significance of these data was subs

Kinetic Study for Reactions of Phenylseleno Radical with Vinyl Monomers

Ito, Osamu

, p. 850 - 853 (2007/10/02)

The reactivities of the phenylseleno radical (PheSe.) generated by flash photolysis of diphenyl diselenide have been determined.Low reactivities of PhSe. toward oxygen, hydrogen -atom donors, and halogen-atom donors have been confirmed.With vinyl monomers (CH2=CHY) PhSe. reacts in a reversible fashion; by the addition of oxygen as a selective radical trap to the adduct radicals (PhSeCH2C.HY), the absolute addition rate constants have been determined.The reverse rate constants and the equilibrium constants have been estimated as relative ones from which the thermodynamic stabilities of the adduct radicals have been elucidated.The addition rates increase mainly with the stabilities of the adduct radicals and subsequently with the polar nature of the transition state.The lower reactivity of PhSe. compared with the phenylthio radical (PhS.) is attributed to the greater stabilization of an unpaired electron in PhSe. than that in PhS..

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