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2-Chloroethyl octanoate is an organic compound with the chemical formula C10H19ClO2. It is a colorless liquid at room temperature and is derived from the esterification of 2-chloroethanol and octanoic acid. 2-chloroethyl octanoate is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive chloroethyl group, it can undergo nucleophilic substitution reactions, making it a valuable building block in organic synthesis. It is also known for its potential use in the preparation of surface-active agents and as a solvent. However, it is important to note that 2-chloroethyl octanoate can be harmful if inhaled, ingested, or absorbed through the skin, and appropriate safety measures should be taken when handling this substance.

589-76-4

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589-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 589-76-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 589-76:
(5*5)+(4*8)+(3*9)+(2*7)+(1*6)=104
104 % 10 = 4
So 589-76-4 is a valid CAS Registry Number.

589-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloroethyl octanoate

1.2 Other means of identification

Product number -
Other names Octanoic acid,2-chloroethyl ester

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:589-76-4 SDS

589-76-4Relevant academic research and scientific papers

PROCESS FOR HYDROCHLORINATION OF MULTIHYDROXYLATED ALIPHATIC HYDROCARBONS

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Page/Page column 21-23, (2011/12/14)

A process for producing a chlorohydrin, an ester of a chlorohydrin, or a mixture thereof including the steps of contacting, in a hydrochlorination reactor, a multihydroxylated aliphatic hydrocarbon, an ester of a multihydroxylated aliphatic hydrocarbon, or a mixture thereof with a source of a hydrogen chloride, in the presence of a hydrophobic or extractable carboxylic acid catalyst is provided.

Acetals oxidation into esters with electrophilic halogens

Mingotaud,Florentin,Marquet

, p. 2401 - 2404 (2007/10/02)

A preparative oxidation of dioxolanes groups into esters is described. Among the different electophilic halogens and solvents which have been tested, ICl/H2O in methylene chloride and Br2/H2O in acetonitrile gave the best results.

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