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79392-43-1

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79392-43-1 Usage

General Description

2,2,2-Trifluoroacetic acid octadecyl ester is a chemical compound that is a derivative of trifluoroacetic acid and octadecyl alcohol. It is an ester with the chemical formula C24H39F3O2 and is commonly used as a reagent in organic synthesis and as a solvent for various chemical reactions. 2,2,2-Trifluoroacetic acid octadecyl ester is a colorless, viscous liquid with a fruity odor, and it is insoluble in water but soluble in organic solvents. It is often used as a stabilizer in the formulation of pesticides, and it can also be used as a solvent for the preparation of pharmaceutical drugs and in chromatography applications. Additionally, this compound is used as a propanol substitute for cleaning and degreasing applications in industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 79392-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,9 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79392-43:
(7*7)+(6*9)+(5*3)+(4*9)+(3*2)+(2*4)+(1*3)=171
171 % 10 = 1
So 79392-43-1 is a valid CAS Registry Number.

79392-43-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name octadecyl 2,2,2-trifluoroacetate

1.2 Other means of identification

Product number -
Other names Acetic acid,trifluoro-,octadecyl 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:79392-43-1 SDS

79392-43-1Relevant articles and documents

A one-pot rapid synthesis of dithiocarbamates from alcohols using a polymer supported diethyl dithiocarbamate anion

Bandgar,Sadavarte,Uppalla

, p. 450 - 451 (2007/10/03)

A polymer supported diethyl dithiocarbamate anion reacts with primary and secondary alcohols via their tirfluoracetates giving alkylated diethyl dithiocarbamates in good yields.

A New and Efficient One-Pot Preparation of Alkyl Halides From Alcohols

Camps, Francisco,Gasol, Vicens,Guerrero, Angel

, p. 511 - 512 (2007/10/02)

Primary alkanols and 2-alkenols are converted into the corresponding halides in high yield by a one-pot, two-step reaction via transformation into intermediate trifluoroacetates followed by nucleophilic substitution with lithium halides.

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