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Ethyl p-tolyl carbonate is a colorless liquid chemical compound with a faint, sweet odor, used as a building block in the synthesis of various organic compounds, including specialty chemicals, pharmaceuticals, and agrochemicals. It is readily soluble in organic solvents and is also utilized in the manufacturing of fragrances and flavors. Ethyl p-tolyl carbonate is considered relatively stable under normal conditions, but proper safety precautions should be followed during handling and storage to prevent potential hazards.

22719-81-9

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22719-81-9 Usage

Uses

Used in Specialty Chemicals Industry:
Ethyl p-tolyl carbonate is used as a building block for the synthesis of various specialty chemicals, contributing to the development of innovative products and materials.
Used in Pharmaceutical Industry:
Ethyl p-tolyl carbonate is employed as a key intermediate in the production of pharmaceuticals, aiding in the creation of new and effective medications.
Used in Agrochemicals Industry:
Ethyl p-tolyl carbonate is utilized in the synthesis of agrochemicals, playing a crucial role in the development of agricultural products that enhance crop protection and yield.
Used in Fragrance and Flavor Industry:
Ethyl p-tolyl carbonate is used as a component in the manufacturing of fragrances and flavors, adding unique scents and tastes to various consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 22719-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,1 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22719-81:
(7*2)+(6*2)+(5*7)+(4*1)+(3*9)+(2*8)+(1*1)=109
109 % 10 = 9
So 22719-81-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-3-12-10(11)13-9-6-4-8(2)5-7-9/h4-7H,3H2,1-2H3

22719-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (4-methylphenyl) carbonate

1.2 Other means of identification

Product number -
Other names Carbonic acid,ethyl p-tolyl 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:22719-81-9 SDS

22719-81-9Relevant academic research and scientific papers

Synthesis, antifungal activity, and molecular docking studies of novel triazole derivatives

Wang, Nan,Chai, Xiaoyun,Chen, Ying,Zhang, Lei,Li, Wenjuan,Gao, Yijun,Bi, Yi,Yu, Shichong,Meng, Qingguo

, p. 384 - 388 (2013/07/28)

In order to meet the urgent need for novel antifungal agents with improved activity and broader spectrum, a series of 3/4-[[N-alkyl-2-(2,4-difluorophenyl)- 2-hydroxy-3-(1H-1, 2, 4-triazole)] propylamino] benzylethyl carbonate were designed, synthesized and evaluated as antifungal agents. The MIC80 values indicate that all the compounds showed only moderate or even no antifungal activities against nearly all the tested fungal pathogens. Moreover, the interactions of the most active compounds in the drug binding site of CACYP51 were also explored with the help of docking studies.

On the reactivity of imidazole carbamates and ureas and their use as esterification and amidation reagents

Heller, Stephen T.,Sarpong, Richmond

experimental part, p. 8851 - 8859 (2011/12/02)

The optimization, substrate scope, and mechanism of esterification and amidation of carboxylic acids mediated by imidazole-based reagents are discussed. The innate reactivity of carbonylimidazole reagents with a range of nucleophiles is also explored. New reagents developed for the synthesis of α,β-unsaturated esters are described, as are reagents for the preparation of tertiary amides directly from carboxylic acids.

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