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Hydroperoxide, 2-phenylcyclohexyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52426-86-5

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52426-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52426-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,2 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52426-86:
(7*5)+(6*2)+(5*4)+(4*2)+(3*6)+(2*8)+(1*6)=115
115 % 10 = 5
So 52426-86-5 is a valid CAS Registry Number.

52426-86-5SDS

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 1-Phenyl-2-hydroperoxy-cyclohexan

1.2 Other means of identification

Product number -
Other names 2-Phenyl-cyclohexyl-hydroperoxide

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:52426-86-5 SDS

52426-86-5Upstream product

52426-86-5Downstream Products

52426-86-5Relevant academic research and scientific papers

Selective catalytic oxidation of cyclohexylbenzene to cyclohexylbenzene-1-hydroperoxide: A coproduct-free route to phenol

Arends, Isabel W.C.E,Sasidharan, Manickam,Kühnle, Adolf,Duda, Mark,Jost, Carsten,Sheldon, Roger A

, p. 9055 - 9061 (2002)

A method is described for the highly selective oxidation of cyclohexylbenzene to cyclohexylbenzene-1-hydroperoxide. In the presence of 0.5mol% N-hydroxyphthalimide (NHPI) and 2mol% of the hydroperoxide product, without solvent, a selectivity of ca. 98% to the desired product was obtained at 32% conversion. The use of NHPI increases the selectivity for initial H-abstraction from the 1-position, vs the other positions in the cyclohexyl ring, suppresses byproduct formation via transannular hydrogen abstraction and increases the overall rate of reaction.

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