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15619-54-2

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15619-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15619-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,1 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15619-54:
(7*1)+(6*5)+(5*6)+(4*1)+(3*9)+(2*5)+(1*4)=112
112 % 10 = 2
So 15619-54-2 is a valid CAS Registry Number.

15619-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butylperoxycyclohexane

1.2 Other means of identification

Product number -
Other names tert-butyl cyclohexyl peroxide

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:15619-54-2 SDS

15619-54-2Downstream Products

15619-54-2Relevant articles and documents

Highly selective cycloalkane oxidation in water with ruthenium nanoparticles

Denicourt-Nowicki, Audrey,Lebedeva, Anastasia,Bellini, Clément,Roucoux, Alain

, p. 357 - 362 (2016/02/05)

Ruthenium(0) nanospecies, with small sizes of approximately 1.75 nm, proved to be active, selective, and retrievable nanocatalysts for the oxidation of various cycloalkanes in neat water, using tert-butylhydroperoxide as an oxidant and at room temperature. Relevant conversions and selectivities (up to 97 %) were achieved towards the major formation of the ketone product, which constitutes a high-value-added intermediate for polymer or fine chemistry. The lifetime of the catalyst has been checked over several runs, with no significant loss of activity and selectivity. Kinetic and mechanistic investigations proved that radical species are involved in the oxidation process. A literature comparison showed the relevance and the usefulness of the present ruthenium nanocatalytic system in a benign reaction context. Active, selective, and retrievable! A sustainable oxidation process of cycloalkanes to the ketones with an easy-to-handle and reusable catalyst, in neat water, and under ambient conditions is described. The active catalyst is a ruthenium(0) nanospecies. t-BHP=tert-butylhydroperoxide.

Selective oxidation of cyclohexane to cyclohexanol catalyzed by a μ-hydroxo diiron(II) complex and tert-butylhydroperoxide

Vincent, Jean-Marc,Bearnais-Barbry, Stephane,Pierre, Celine,Verlhac, Jean-Baptiste

, p. 1913 - 1914 (2007/10/03)

A new μ-hydroxo diiron(II) complex [Fe2L(OH)]3+ obtained with a dinucleating macrocyclic ligand catalyzes the selective oxidation of cyclohexane into cyclohexanol (≈85%) using the controlled addition of tert-butylhydroperoxide.

Ruthenium colloids: A new catalyst for alkane oxidation by tBHP in a biphasic water-organic phase system

Launay, Franck,Roucoux, Alain,Patin, Henri

, p. 1353 - 1356 (2007/10/03)

Efficient and highly selective conversion of cyclooctane into cyclooctanone is obtained under pure biphasic conditions through t-butylhydroperoxide activation by the in situ formation of colloidal ruthenium species arising from RuCl3, 3H2O. Model extension experiments to other cycloalkanes are also discussed.

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