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Benzeneacetic acid, a-phenyl-, 2,2,2-trichloroethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94598-40-0

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94598-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94598-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,9 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 94598-40:
(7*9)+(6*4)+(5*5)+(4*9)+(3*8)+(2*4)+(1*0)=180
180 % 10 = 0
So 94598-40-0 is a valid CAS Registry Number.

94598-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trichloroethyl diphenylacetate

1.2 Other means of identification

Product number -
Other names Diphenyl-acetic acid 2,2,2-trichloro-ethyl 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:94598-40-0 SDS

94598-40-0Relevant academic research and scientific papers

A Simple and Mild Esterification Method for Carboxylic Acids Using Mixed Carboxylic-Carbonic Anhydrides

Kim, Sunggak,Lee, Jae In,Kim, Youn Chul

, p. 560 - 565 (1985)

A simple and mild esterification method using mixed carboxylic-carbonic anhydrides has been developed.Simple aliphatic carboxylic esters are prepared in high yields by the reaction of acids with equimolar amounts of chloroformates (2,2,2-trichloroethyl chloroformate is an exception) and triethylamine in the presence of a catalytic amount of 4-(dimethylamino)pyridine.Although aromatic acids give a mixture of the ester, the acid anhydride, and the carbonate under normal conditions utilized in this study, it is found that increasing the amount of 4-(dimethylamino)pyridine drastically decreases the formation of the acid anhydride and the carbonate, affording a satisfactory yield of the ester.This method reaches a limit with sterically hindered acids and the formation of the acid anhydride and the carbonate is favored.

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