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122-45-2

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122-45-2 Usage

Description

Octyl phenylacetate has a pleasant, slightly fatty, citrus-like odor. May be prepared by esterification of n-octanol with phenylacetic acid.

Chemical Properties

n-Octyl phenylacetate has a pleasant, mild sweet-floral odor of woody–orange–rose type.

Preparation

By esterification of n-octanol with phenylacetic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 122-45-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122-45:
(5*1)+(4*2)+(3*2)+(2*4)+(1*5)=32
32 % 10 = 2
So 122-45-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H24O2/c1-2-3-4-5-6-10-13-18-16(17)14-15-11-8-7-9-12-15/h7-9,11-12H,2-6,10,13-14H2,1H3

122-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name octyl 2-phenylacetate

1.2 Other means of identification

Product number -
Other names n-octyl phenylacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:122-45-2 SDS

122-45-2Relevant articles and documents

ZWITTERIONIC CATALYSTS FOR (TRANS)ESTERIFICATION: APPLICATION IN FLUOROINDOLE-DERIVATIVES AND BIODIESEL SYNTHESIS

-

Paragraph 0015; 0028, (2021/01/29)

An amide/iminium zwitterion catalyst has a catalyst pocket size that promotes transesterification and dehydrative esterification. The amide/iminium zwitterions are easily prepared by reacting aziridines with aminopyridines. The reaction can be applied a wide variety of esterification processes including the large-scale synthesis of biodiesel. The amide/iminium zwitterions allow the avoidance of strongly basic or acidic condition and avoidance of metal contamination in the products. Reactions are carried out at ambient or only modestly elevated temperatures. The amide/iminium zwitterion catalyst is easily recycled and reactions proceed in high to quantitative yields.

Amide/Iminium Zwitterionic Catalysts for (Trans)esterification: Application in Biodiesel Synthesis

Lam, Ying-Pong,Ng, Wing-Hin,Tan, Fei,Tse, Ying-Lung Steve,Wang, Xinyan,Yeung, Ying-Yeung

, p. 8083 - 8092 (2019/08/26)

A class of zwitterionic organocatalysts based on an amide anion/iminium cation charge pair has been developed. The zwitterions are easily prepared by reacting aziridines with aminopyridines. They are catalytically applicable to transesterifications and dehydrative esterifications. Mechanistic studies reveal that the amide anion and iminium cation work synergistically in activating the reaction partners, with the iminium cationic moiety interacting with the carbonyl substrates through nonclassical hydrogen bonding. The reaction can be applied to large-scale synthesis of biodiesel under mild conditions.

CeO2 as a versatile and reusable catalyst for transesterification of esters with alcohols under solvent-free conditions

Tamura, Masazumi,Hakim Siddiki,Shimizu, Ken-Ichi

, p. 1641 - 1646 (2013/09/24)

CeO2 acted as an efficient and reusable heterogeneous catalyst for transesterification of esters with alcohols under the solvent-free conditions at 160 °C. Among the 11 kinds of metal oxides, CeO2 is the most suitable catalyst in terms of catalytic activity, leaching-resistance and reusability. This catalytic system tolerates various esters and alcohols, and valuable esters such as heteroaromatic esters and benzyl benzoates are produced, demonstrating a practical utility of the system. On the basis of kinetic analysis and in situ IR studies of adsorbed species, a reaction mechanism is proposed, in which proton abstraction of alcohol by a Lewis base site of CeO2 to yield alkoxide species is the rate-limiting step.

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