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ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE is a chemical compound with the molecular formula C11H11Cl2O3, characterized by its pale yellow liquid form and a fruity odor. It is a derivative of ethyl 3-oxopropionate, featuring two chlorine atoms attached to a benzene ring, which contributes to its diverse industrial applications.

72835-87-1

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72835-87-1 Usage

Uses

Used in Pharmaceutical Industry:
ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the development of new drugs, enhancing their therapeutic properties and effectiveness in treating various medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE serves as an essential component in the production of various agrochemicals. Its presence in these compounds contributes to their pesticidal, herbicidal, or insecticidal properties, helping to protect crops and improve agricultural yields.
Used in Organic Compound Production:
ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE is also utilized as an intermediate in the production of other organic compounds. Its versatile chemical structure makes it a valuable building block for creating a wide range of organic molecules with various applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 72835-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,3 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72835-87:
(7*7)+(6*2)+(5*8)+(4*3)+(3*5)+(2*8)+(1*7)=151
151 % 10 = 1
So 72835-87-1 is a valid CAS Registry Number.

72835-87-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE

1.2 Other means of identification

Product number -
Other names 2,6-Dichloro-beta-Oxo-Benzenepropanoic Acid 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:72835-87-1 SDS

72835-87-1Relevant academic research and scientific papers

MOLECULES HAVING PESTICIDAL UTILITY, AND INTERMEDIATES, COMPOSITIONS, AND PROCESSES, RELATED THERETO

-

Page/Page column 106; 107, (2016/07/05)

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, compositions containing such molecules, and processes of using such molecules and compositions against such pests. These molecules and compositions may be used, for example, as acaricides, insecticides, miticides, molluscicides, and nematicides. This document discloses molecules having the following formula ("Formula One").

Discovery of potent and selective pyrazolopyrimidine Janus kinase 2 inhibitors

Hanan, Emily J.,Van Abbema, Anne,Barrett, Kathy,Blair, Wade S.,Blaney, Jeff,Chang, Christine,Eigenbrot, Charles,Flynn, Sean,Gibbons, Paul,Hurley, Christopher A.,Kenny, Jane R.,Kulagowski, Janusz,Lee, Leslie,Magnuson, Steven R.,Morris, Claire,Murray, Jeremy,Pastor, Richard M.,Rawson, Tom,Siu, Michael,Ultsch, Mark,Zhou, Aihe,Sampath, Deepak,Lyssikatos, Joseph P.

, p. 10090 - 10107 (2013/01/16)

The discovery of somatic Jak2 mutations in patients with chronic myeloproliferative neoplasms has led to significant interest in discovering selective Jak2 inhibitors for use in treating these disorders. A high-throughput screening effort identified the p

Cyclic Amidines Part 25. Intramolecular Cyclodehalogenation of Diazabenzanthracenes and Diazabenzophenanthrenes

Bloomfield, Derek G.,Upton, Christopher,Vipond, Hilton J.

, p. 857 - 860 (2007/10/02)

A previously unrecorded intramolecular cyclization which occurred during the palladium-catalysed hydrogenolysis of suitably disposed dichloroheterocycles anthracene (3) to 9,14-diazabenzaceanthrylene

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