72835-87-1

Basic information

• Product Name: ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE
• Synonyms: ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE;Ethyl 3-(2,6-dichlorophenyl)
• CAS NO: 72835-87-1
• Molecular Formula: C₁₁H₁₀Cl₂O₃
• Molecular Weight: 261.1
• Mol File: 72835-87-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 290.6 °C at 760 mmHg
• Flash Point: 109.7 °C
• Appearance: /
• Density: 1.319 g/cm³
• Storage Temp.: 2-8°C
• PKA: 9.85±0.50(Predicted)
• CAS DataBase Reference: ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE(72835-87-1)
• EPA Substance Registry System: ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE(72835-87-1)

Safety Data

• Hazardous Substances Data: 72835-87-1(Hazardous Substances Data)

Usage

General Description

ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE is a chemical compound with the molecular formula C11H11Cl2O3. It is a derivative of ethyl 3-oxopropionate and contains two chlorine atoms attached to a benzene ring. ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE is commonly used in the synthesis of various pharmaceuticals and agrochemicals. It is also used as an intermediate in the production of other organic compounds. ETHYL 3-(2,6-DICHLOROPHENYL)-3-OXOPROPANOATE is a pale yellow liquid with a fruity odor and has a variety of industrial applications.

Upstream product

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Downstream Products

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Relevant articles and documents

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

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").

Cyclic Amidines Part 25. Intramolecular Cyclodehalogenation of Diazabenzanthracenes and Diazabenzophenanthrenes

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