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20618-90-0

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20618-90-0 Usage

Derived from

1,2-propanediol (glycerol)

Chlorinated derivative

Yes

Physical state

Colorless liquid

Odor

Slightly sweet

Uses

Solvent, reagent in organic synthesis

Skin irritation

Yes

Eye irritation

Yes

Respiratory system irritation

Yes

Safety precautions

Handle with caution and follow proper safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 20618-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,1 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20618-90:
(7*2)+(6*0)+(5*6)+(4*1)+(3*8)+(2*9)+(1*0)=90
90 % 10 = 0
So 20618-90-0 is a valid CAS Registry Number.

20618-90-0SDS

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 1-(chloromethyl)-2-hydroxyethyl acetate

1.2 Other means of identification

Product number -
Other names acetic acid-(β-chloro-β'-hydroxy-isopropyl 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:20618-90-0 SDS

20618-90-0Downstream Products

20618-90-0Relevant articles and documents

The solvent effects in the reactions of carboxylic acids with oxiranes. 1. Kinetics of the reaction of acetic acid with epichlorohydrin in butan-1-ol

Bukowski, Wiktor

, p. 378 - 387 (2007/10/03)

Kinetics of the reaction of acetic acid with epichlorohydrin in the presence of chromium(III) acetate in butan-1-ol solution have been studied. The partial reaction orders with respect to reagents were found. The reactions were of first-order with respect to both epichlorohydrin and catalyst and zeroth order with respect to acetic acid. A kinetic model for the overall process has been proposed. The reaction constants have been calculated along with the activation parameters. The effect of dilution on the rate of addition is discussed. In the equimolar mixture of acetic acid and epichlorohydrin the apparent rate constant of the addition k1 initially decreases to increase again at the concentration of butan-1-ol exceeding 3 M.

A Convenient Synthesis of Glycidyl Esters (2,3-Epoxypropyl Alkanoates)

Otera, Junzo,Matsuzaki, Shinjiro

, p. 1019 - 1020 (2007/10/02)

A novel method for synthesizing glycidyl esters (2,3-epoxypropyl alkanoates) 1 has been achieved by the sequence of the organotin phosphate catalyzed reaction of epichlorohydrin 2 with carboxylic acids and dehydrochlorination of the resulting mixture of ester chlorohydrins 3 + 4 followed by separation.

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