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1-chloropropan-2-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

623-60-9

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623-60-9 Usage

Physical state

Colorless liquid

Odor

Pungent

Usage

Reagent in organic synthesis

Key intermediate

Production of allylbenzene

Applications

a. Manufacture of polymers
b. Precursor to other chemicals
c. Flavor and fragrance agent in food and beverage industry

Safety precautions

Flammable and irritant substance, handle with caution

Check Digit Verification of cas no

The CAS Registry Mumber 623-60-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 623-60:
(5*6)+(4*2)+(3*3)+(2*6)+(1*0)=59
59 % 10 = 9
So 623-60-9 is a valid CAS Registry Number.

623-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloropropan-2-yl acetate

1.2 Other means of identification

Product number -
Other names 1-chloro-2-acetoxypropane

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:623-60-9 SDS

623-60-9Downstream Products

623-60-9Relevant academic research and scientific papers

CONVERSION OF A MULTIHYDROXYLATED-ALIPHATIC HYDROCARBON OR ESTER THEREOF TO A CHLOROHYDRIN

-

Page/Page column 37-38, (2008/06/13)

The present invention relates to a process for converting a multihydroxylated-aliphatic hydrocarbon or ester thereof to a chlorohydrin, by contacting the multihydroxylated-aliphatic hydrocarbon or ester thereof starting material with a source of a superatmospheric partial pressure of hydrogen chloride for a sufficient time and at a sufficient temperature, and wherein such contracting step is carried out without substantial removal of water, to produce the desired chlorohydrin product; wherein the desired product or products can be made in high yield without substantial formation of undesired overchlorinated byproducts. In addition, certain catalysts of the present invention may be used in the present process at superatmospheric, atmospheric and subatmospheric pressure conditions with improved results.

Reactions du n=chloroparatoluenesulfonamidate de sodium (chloramine t) sur les olefines en miliu acide organique

Damin, Bernard,Garapon, Jacques,Sillion, Bernard

, p. 1709 - 1710 (2007/10/02)

Vic. chloro-acetoxy and vic. chloro-tosylamino alcanes are the main products of the electrophilic reaction of chloramine T on olefins in acetic acid. The stereochemistry of the acetoxy chloration of the 2-butenes and cyclohexene is trans.

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