141852-65-5

Basic information

• Product Name: 2-CHLORO-4-FLUOROPHENOL CARBONATE
• Synonyms: 2-CHLORO-4-FLUOROPHENOL CARBONATE;2-Chloro-4-fluorophenyl hydrogen carbonate
• CAS NO: 141852-65-5
• Molecular Formula: C₁₃H₆Cl₂F₂O₃
• Molecular Weight: 190.56
• Mol File: 141852-65-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 362.4°C at 760 mmHg
• Flash Point: 142.3°C
• Appearance: /
• Density: 1.51g/cm³
• Vapor Pressure: 1.94E-05mmHg at 25°C
• Refractive Index: 1.566
• CAS DataBase Reference: 2-CHLORO-4-FLUOROPHENOL CARBONATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-4-FLUOROPHENOL CARBONATE(141852-65-5)
• EPA Substance Registry System: 2-CHLORO-4-FLUOROPHENOL CARBONATE(141852-65-5)

Safety Data

• Hazardous Substances Data: 141852-65-5(Hazardous Substances Data)

Usage

General Description

2-Chloro-4-fluorophenol carbonate is a chemical compound with the molecular formula C7H5ClFO3. It is a carbonate ester of 2-chloro-4-fluorophenol and is mainly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 2-CHLORO-4-FLUOROPHENOL CARBONATE is a white crystalline solid with a molecular weight of 188.57 g/mol. It is also known by the trade names Dichlorphos and Ebasil. 2-Chloro-4-fluorophenol carbonate is primarily used as a building block for the synthesis of biologically active compounds and can be used in the production of antifungals and herbicides. It is important to handle this compound with care as it is toxic if ingested or inhaled, and can cause skin and eye irritation upon contact.

InChI:InChI=1/C13H6Cl2F2O3/c14-9-5-7(16)1-3-11(9)19-13(18)20-12-4-2-8(17)6-10(12)15/h1-6H

Upstream product

• 1996-41-4 2-chloro-4-fluorophenol 
• 503-38-8 trichloromethyl chloroformate 

Downstream Products

• 124347-13-3 bis(2-chloro-4-fluoro-5-nitrophenyl)carbonate 

Relevant articles and documents

Tetrahydrophthalamide derivative, intermediate for producing the same, production of both, and herbicide containing the same as active ingredient

The present invention relates to 3,4,5,6-tetrahydrophthalamide derivatives and 3,4,5,6-tetrahydroisophthalimide derivatives having excellent effects as effective active ingredients of herbicides, and processes for preparing the same, and provides the compounds having a more efficient herbicidal activity, and efficient and industrial processes for the preparation thereof. More specifically, the tetrahydrophthalimide derivative obtained by reacting a halogen-substituted 5-cycloalkyloxyaniline derivative with a 3,4,5,6-tetrahydrophthalic anhydride, or the tetrahydroisophthalimide derivative of the present invention is reacted with various types of amines to prepare a tetrahydrophthalamide derivative represented by the general formula (I): STR1 These tetrahydrophthalamide derivatives and the tetrahydroisophthalimide derivatives exhibit excellent herbicidal activities in the soil treatment in the paddy field and field and the stem-foliar treatment. The tetrahydroisophthalimide derivatives are also useful as intermediates for the preparation of the tetrahydrophthalamide derivatives, etc.