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Cycloheptanone, 2-(benzoyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53429-51-9

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53429-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53429-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,2 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53429-51:
(7*5)+(6*3)+(5*4)+(4*2)+(3*9)+(2*5)+(1*1)=119
119 % 10 = 9
So 53429-51-9 is a valid CAS Registry Number.

53429-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Benzoyloxy)cycloheptanone

1.2 Other means of identification

Product number -
Other names 2-benzoyloxy cycloheptanone

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:53429-51-9 SDS

53429-51-9Downstream Products

53429-51-9Relevant academic research and scientific papers

One-pot synthesis of α-acyloxycarbonyl compounds via oxidative decarboxylation coupling reaction of α-oxo carboxylic acids with carbonyl compounds

Chang, Li-Ming,Yuan, Gao-Qing

, p. 7003 - 7007 (2016/10/13)

With tetrabutylammonium iodide (TBAI) as the catalyst and tert-butyl hydroperoxide (TBHP) as the oxidant, a simple metal-free protocol has been developed for the synthesis of α-acyloxycarbonyl compounds from carbonyl compounds and α-oxo carboxylic acids via decarboxylative coupling reaction. The target products could be obtained in moderate to high yields.

A general method for the α-acyloxylation of carbonyl compounds

Beshara, Cory S.,Hall, Adrian,Jenkins, Robert L.,Jones, Kerri L.,Jones, Teyrnon C.,Killeen, Niall M.,Taylor, Paul H.,Thomas, Stephen P.,Tomkinson, Nicholas C. O.

, p. 5729 - 5732 (2007/10/03)

(Chemical Equation Presented) A simple, one-pot method for the α-acyloxylation of carbonyl compounds that proceeds at room temperature in the presence of both moisture and air has been developed. Treatment of a variety of aldehydes and both cyclic and acy

Reaction of Enol Silyl Ethers with Silver Carboxylate-Iodine. Synthesis of α-Acyloxy Carbonyl Compounds

Rubottom, George M.,Mott, Robert C.,Juve, Henrik D.

, p. 2717 - 2721 (2007/10/02)

The sequential treatment of enol silyl ethers with silver carboxylate-iodine (2:1) and then fluoride affords high yields of the corresponding α-acyloxy carbonyl compounds.Thus a wide range of variation is now possible for the acyloxy portion of the molecu

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