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6222-35-1

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6222-35-1 Usage

Description

Cyclohexyl propionate is a synthetic flavoring agent that is a stable, colorless liquid with a fruity odor.

Uses

Used in Food Industry:
Cyclohexyl propionate is used as a flavoring agent for fruit flavors such as pineapple in beverages, candy, ice cream, and baked goods at approximately 3 ppm. It provides a fruity aroma and taste to these products, enhancing their overall flavor profile.

Preparation

By direct esterification of the alcohol with the acid in the presence of concentrated sulfuric acid or in the presence of benzene.

Check Digit Verification of cas no

The CAS Registry Mumber 6222-35-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6222-35:
(6*6)+(5*2)+(4*2)+(3*2)+(2*3)+(1*5)=71
71 % 10 = 1
So 6222-35-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c1-2-9(10)11-8-6-4-3-5-7-8/h8H,2-7H2,1H3

6222-35-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclohexyl Propionate

1.2 Other means of identification

Product number -
Other names Propanoic acid, cyclohexyl ester

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:6222-35-1 SDS

6222-35-1Relevant articles and documents

Consecutive addition esterification and hydrolysis of cyclic olefins catalyzed by multi-SO3H functionalized multi heteropolyanion-based ionic hybrids undersolvent-free conditions

Zheng, Guocai,Li, Xinzhong

, p. 933 - 941 (2019/03/17)

An efficient protocol for the synthesis of cycloalkyl carboxylates and alcohols from cyclic olefins is described. The cyclic olefins were converted to corresponding target molecules under solvent-free conditions catalyzed by two novel multi-SO3H functionalized multi heteropolyanion-based ionic hybrids through one-pot consecutive addition esterification and hydrolysis reactions. This approach has several advantages, including high yield, simple workup and simple purification.

Efficient Palladium-Catalyzed Alkoxycarbonylation of Bulk Industrial Olefins Using Ferrocenyl Phosphine Ligands

Dong, Kaiwu,Sang, Rui,Fang, Xianjie,Franke, Robert,Spannenberg, Anke,Neumann, Helfried,Jackstell, Ralf,Beller, Matthias

supporting information, p. 5267 - 5271 (2017/04/27)

The development of ligands plays a key role and provides important innovations in homogeneous catalysis. In this context, we report a novel class of ferrocenyl phosphines for the alkoxycarbonylation of industrially important alkenes. A basic feature of our ligands is the combination of sterically hindered and amphoteric moieties on the P atoms, which leads to improved activity and productivity for alkoxycarbonylation reactions compared to the current industrial state-of-the-art ligand 1,2-bis((di-tert-butylphosphino)methyl)benzene). Advantageously, palladium catalysts with these novel ligands also enable such transformations without additional acid under milder reaction conditions. The practicability of the optimized ligand was demonstrated by preparation on >10 g scale and its use in palladium-catalyzed carbonylations on kilogram scale.

Graphite oxide as an efficient solid reagent for esterification reactions

Mirza-Aghayan, Maryam,Rahimifard, Mahshid,Boukherroub, Rabah

, p. 859 - 864 (2014/12/10)

Esterification of organic acids with alcohols under mild conditions in high yields using graphite oxide, a readily available and inexpensive material, as an effective reagent is described.

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