63418-08-6

Basic information

• Product Name: 2,6-DICHLORO-3,5-DIFLUOROPHENOL
• Synonyms: 2,6-DICHLORO-3,5-DIFLUOROPHENOL
• CAS NO: 63418-08-6
• Molecular Formula: C₆H₂Cl₂F₂O
• Molecular Weight: 198.98
• Product Categories: Phenol&Thiophenol&Mercaptan
• Mol File: 63418-08-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 47-50°C
• Boiling Point: 87 °C
• Flash Point: 80.9 °C
• Appearance: /
• Density: 1.655 g/cm³
• Vapor Pressure: 0.135mmHg at 25°C
• Refractive Index: 1.531
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2,6-DICHLORO-3,5-DIFLUOROPHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DICHLORO-3,5-DIFLUOROPHENOL(63418-08-6)
• EPA Substance Registry System: 2,6-DICHLORO-3,5-DIFLUOROPHENOL(63418-08-6)

Safety Data

• Hazard Codes: C,Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 63418-08-6(Hazardous Substances Data)

Usage

General Description

2,6-Dichloro-3,5-difluorophenol is a compound classified as a chlorinated phenol with two chlorine atoms and two fluorine atoms attached to a phenolic ring. It is commonly used as a pesticide and antimicrobial agent, as well as in the production of pharmaceuticals and other organic compounds. This chemical is known to have antimicrobial properties and is used in a variety of industrial and agricultural applications. However, it is also considered to be toxic to aquatic organisms and may have negative environmental impacts if not properly controlled and regulated. Therefore, proper handling and disposal methods are necessary to minimize the potential risks associated with this chemical.

InChI:InChI=1/C6H2Cl2F2O/c7-4-2(9)1-3(10)5(8)6(4)11/h1,11H

Downstream Products

• 121555-67-7 2,6-Dichloro-3,5-difluoro-4-nitro-phenol 
• 1204677-44-0 (S)-3-[(R)-(2,6-dichloro-3,5-difluorophenoxy)phenyl-methyl]pyrrolidine-1-carboxylic acid t-butyl ester 
• 1165952-91-9 cyclohexa-1,3-diene 
• 877400-00-5 trifluoro-methanesulfonic acid 2,6-dichloro-3,5-difluoro-phenyl ester 

Relevant articles and documents

Fungicidal carbocyclic anilide carbamates

Fungicidal carbocyclic anilide carbamates of the formula STR1 in which X represents optionally alkyl-substituted cycloalkyl or optionally alkyl-substituted cycloalkenyl, Hal represents halogen, and Y1, Y2 and Y3 independently of one another represent hydrogen, halogen, optionally halogen-substituted alkyl, optionally halogen-substituted alkoxy or optionally halogen-substituted alkylthio, and R1 represents optionally halogen-substituted alkyl, alkenyl, alkylcarbonyloxyalkyl, alkenylcarbonyloxyalkyl and optionally substituted cycloalkyl which can be interrupted by hetero atoms, or represents optionally substituted phenyl or optionally substituted phenylalkyl, or R1 additionally can represent alkoxyalkyl, alkylthioalkyl or polyalkoxyalkyl if X represents optionally alkyl-substituted cycloalkenyl.

Fungicidal derivatives of carbocyclic anilides

Fungicidal derivatives of carboxyclic anilides of the formula STR1 in which X represent optionally alkyl-substituted cycloalkyl or optionally alkyl-substituted cycloalkenyl, Hal represents halogen, and Y1, Y2 and Y3 independently of one another represent hydrogen, halogen, optionally halogen-substituted alkyl, optionally halogen-substituted alkoxy or optionally halogen-substituted alkylthio, and Z represents the groups COOR2 or COR1, where R1 and R2 are identical or different and represent optionally halogen-substituted alkyl, alkenyl, alkoxyalkyl, alkylthioalkyl, polyalkoxyalkyl and optionally substituted cycloalkyl, optionally substituted phenyl, optionally substituted phenylalkyl or substituted phenoxyalkyl.

Substituted aminophenyl carbamates

Fungicidal substituted aminophenyl carbamates of the formula STR1 in which X represents --CO--NR8 R9 ; --CO--OR9 ; --CO--SR9 ; --COR10 ; --SO2 R9 or hydrogen, in which