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2,6-DICHLORO-3,5-DIFLUOROPHENOL is a chlorinated phenol compound characterized by the presence of two chlorine and two fluorine atoms attached to a phenolic ring. It is recognized for its antimicrobial properties and is utilized in various industrial and agricultural applications, including as a pesticide and antimicrobial agent. However, it is also acknowledged for its potential toxicity to aquatic organisms, necessitating careful handling and disposal to mitigate environmental risks.

63418-08-6

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63418-08-6 Usage

Uses

Used in Pesticide Industry:
2,6-DICHLORO-3,5-DIFLUOROPHENOL is used as an active ingredient for its pesticidal properties, leveraging its ability to control, prevent, or kill pests. Its effectiveness in this application is attributed to its antimicrobial action, which helps protect crops from diseases and infestations.
Used in Antimicrobial Applications:
In various settings, 2,6-DICHLORO-3,5-DIFLUOROPHENOL is used as a sanitizing and disinfecting agent due to its antimicrobial capabilities. This application is crucial in environments where the control of microbial growth is essential for maintaining hygiene and preventing the spread of diseases.
Used in Pharmaceutical Production:
2,6-DICHLORO-3,5-DIFLUOROPHENOL is utilized as a key intermediate in the synthesis of certain pharmaceuticals. Its chemical structure allows it to be a building block for the development of drugs that may have therapeutic applications in medicine.
Used in Organic Compounds Synthesis:
2,6-DICHLORO-3,5-DIFLUOROPHENOL serves as a precursor in the production of other organic compounds, contributing to the synthesis of various chemical entities that find use in different industries, such as the chemical and materials science sectors.
Environmental Considerations:
Given its potential toxicity to aquatic organisms, 2,6-DICHLORO-3,5-DIFLUOROPHENOL requires careful management to prevent negative environmental impacts. Proper handling, storage, and disposal methods are essential to ensure that its use does not lead to ecological harm. Regulatory measures and industry best practices should be adhered to in order to minimize the chemical's release into the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 63418-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,1 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63418-08:
(7*6)+(6*3)+(5*4)+(4*1)+(3*8)+(2*0)+(1*8)=116
116 % 10 = 6
So 63418-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H2Cl2F2O/c7-4-2(9)1-3(10)5(8)6(4)11/h1,11H

63418-08-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-DICHLORO-3,5-DIFLUOROPHENOL

1.2 Other means of identification

Product number -
Other names 2,5-DIACETOACETAMIDO BENZENE SULFONIC ACID

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:63418-08-6 SDS

63418-08-6Upstream product

63418-08-6Relevant academic research and scientific papers

Fungicidal carbocyclic anilide carbamates

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, (2008/06/13)

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.

Acylated aminophenol derivatives

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, (2008/06/13)

There are described cycloalkyl-carboxanilides of the formula (I) STR1 in which X, Hal, Y1, Y2, Y3 and Z have the meaning given in the description, and a process for their preparation. The compounds of the formula (I) are used for combating pests.

Fungicidal derivatives of carbocyclic anilides

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, (2008/06/13)

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 cycloalkyl- and heterocyclyl-carboxanilides

-

, (2008/06/13)

A substituted cycloalkyl- or heterocyclyl-carboxanilide of the formula (I) STR1 in which X stands for an unsubstituted or an alkyl-substituted cycloalkyl or an unsubstituted or an alkyl-substituted heterocyclic, Hal stands for halogen and Y1, Y

Substituted aminophenyl carbamates

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, (2008/06/13)

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

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