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10052-96-7

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10052-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10052-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,5 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10052-96:
(7*1)+(6*0)+(5*0)+(4*5)+(3*2)+(2*9)+(1*6)=57
57 % 10 = 7
So 10052-96-7 is a valid CAS Registry Number.

10052-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name phosphorosobenzene

1.2 Other means of identification

Product number -
Other names Phosphine oxide,phenyl

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:10052-96-7 SDS

10052-96-7Relevant academic research and scientific papers

benzyl pair (2, 4, 6-trimethyl benzoyl) phosphine oxide of the preparation method

-

, (2016/11/21)

The invention discloses a preparation method of phenyl bis(2,4,6-trimethylbenzoyl)phosphine oxide as an efficient free radical photoinitiator. The preparation method of phenyl bis(2,4,6-trimethylbenzoyl)phosphine oxide comprises the concrete steps of with 2,4,6-trimethylbenzaldehyde as a raw material, enabling 2,4,6-trimethylbenzaldehyde and phenylphosphine oxide to be subjected to condensation reaction in the existence of a catalyst, and then, carrying out oxidation reaction. Extraction and solvent replacement are not needed and continuous reaction can be realized in the reaction process. The preparation method of phenyl bis(2,4,6-trimethylbenzoyl)phosphine oxide, disclosed by the invention, is low in price, environment-friendly, easy to operate and suitable for realizing industrialization.

Remarkably robust monomeric alkylperoxyzinc compounds from tris(oxazolinyl)boratozinc alkyls and O2

Mukherjee, Debabrata,Ellern, Arkady,Sadow, Aaron D.

scheme or table, p. 13018 - 13026 (2012/10/08)

Metal alkylperoxides are remarkable, highly effective, yet often thermally unstable, oxidants that may react through a number of possible pathways including O-O homolytic cleavage, M-O homolytic cleavage, nucleophilic O-atom transfer, and electrophilic O-atom transfer. Here we describe a series of zinc alkyl compounds of the type ToMZnR (ToM = tris(4,4-dimethyl-2-oxazolinyl)phenylborate; R = Et, n-C3H 7, i-C3H7, t-Bu) that react with O2 at 25 °C to form isolable monomeric alkylperoxides ToMZnOOR in quantitative yield. The series of zinc alkylperoxides is crystallographically characterized, and the structures show systematic variations in the Zn-O-O angle and O-O distances. The observed rate law for the reaction of ToMZnEt (2) and O2 is consistent with a radical chain mechanism, where the rate-limiting SH2 step involves the interaction of ?OOR and ToMZnR. In contrast, ToMZnH and ToMZnMe are unchanged even to 120 °C under 100 psi of O 2 and in the presence of active radical chains (e.g., ?OOEt). This class of zinc alkylperoxides is unusually thermally robust, in that the compounds are unchanged after heating at 120 °C in solution for several days. Yet, these compounds are reactive as oxidants with phosphines. Additionally, an unusual alkylperoxy group transfer to organosilanes affords ToMZnH and ROOSiR3'.

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