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20387-24-0

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20387-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20387-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,8 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20387-24:
(7*2)+(6*0)+(5*3)+(4*8)+(3*7)+(2*2)+(1*4)=90
90 % 10 = 0
So 20387-24-0 is a valid CAS Registry Number.

20387-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Peroxidradikal v. Diphenylmethan

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:20387-24-0 SDS

20387-24-0Relevant articles and documents

-

Howard,J.A.,Ingold,K.U.

, p. 1056 - 1058 (1968)

-

Quenching of singlet oxygen by oxygen- and sulfur-centered radicals: Evidence for energy transfer to peroxyl radicals in solution

Darmanyan, Alexandre P.,Gregory, Daniel D.,Guo, Yushen,Jenks, William S.,Burel, Laure,Eloy, Dominique,Jardon, Pierre

, p. 396 - 403 (2007/10/03)

Quenching of singlet oxygen luminescence at 1.27 μm by PhS., PhSO., and peroxyl radicals PhOO., t-BuOO., PhCH2OO., Ph2CHOO. and Ph3COO. was studied in liquid solution. The quantum yields of decomposition of different initiators which lead to the formation of free radicals were measured by using nanosecond transient absorption. This allowed determination of singlet oxygen O2(1Δ(g)) quenching rate constants by the radicals. They are 8 M-1 s-1 for the sulfur-centered radicals and (2-7) x 109 M-1 s-1 for peroxyl radicals in acetonitrile. The rapid quenching is attributed to energy transfer quenching by the peroxyls, which have an n → π* transition leading to a low-lying 2A' state above their 2A'' ground state. PhSO. is shown computationally not to have such a low-lying 2A' state. There may be a very low-lying 2B1 state, for PhS., but it is apparently not an efficient acceptor of electronic energy from O2(1Δ(g)).

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