57000-78-9

Basic information

• Product Name: 1-(4-CHLOROPHENOXY)-3,3-DIMETHYL-1-CHLORO-2-BUTANONE
• Synonyms: 1-(4-CHLOROPHENOXY)-1-CHLORO-3,3-DIMETHYL-2-BUTANONE;1-(4-CHLOROPHENOXY)-3,3-DIMETHYL-1-CHLORO-2-BUTANONE;2-Butanone, 1-chloro-1-(4-chlorophenoxy)-3,3-dimethyl-;3,3-dimethyl-1-chloro-1-(4-Chlorophenoxy)butan-2-one;Chlorophenoxy dimethyl chloro butanone;1-Chloro-1-(4-chlorophenoxy)-3,3-diMethylbutan-2-one
• CAS NO: 57000-78-9
• Molecular Formula: C12H14Cl2O2
• Molecular Weight: 261.14
• EINECS: 1533716-785-6
• Mol File: 57000-78-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 328.9 °C at 760 mmHg
• Flash Point: 126.2 °C
• Appearance: /
• Density: 1.204 g/cm³
• Vapor Pressure: 0.000183mmHg at 25°C
• Refractive Index: 1.518
• CAS DataBase Reference: 1-(4-CHLOROPHENOXY)-3,3-DIMETHYL-1-CHLORO-2-BUTANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-CHLOROPHENOXY)-3,3-DIMETHYL-1-CHLORO-2-BUTANONE(57000-78-9)
• EPA Substance Registry System: 1-(4-CHLOROPHENOXY)-3,3-DIMETHYL-1-CHLORO-2-BUTANONE(57000-78-9)

Safety Data

• Hazardous Substances Data: 57000-78-9(Hazardous Substances Data)

Usage

General Description

"1-(4-Chlorophenoxy)-3,3-dimethyl-1-chloro-2-butanone" is a chemical compound that is used as a herbicide and pesticide. It is a selective herbicide that is commonly used to control broadleaf weeds in agricultural and horticultural crops. With its selective nature, it targets specific weed species while leaving desirable crops unaffected. This chemical works by inhibiting the growth of weeds and interfering with their ability to photosynthesize, ultimately leading to their death. Due to its potential health and environmental risks, proper handling and precautionary measures should be taken when using this chemical.

InChI:InChI=1/C12H14Cl2O2/c1-12(2,3)10(15)11(14)16-9-6-4-8(13)5-7-9/h4-7,11H,1-3H3

Upstream product

• 106-48-9 4-chloro-phenol 
• 24473-06-1 1-(4'-chlorophenoxy)-3,3-dimethyl-butan-2-one 
• 75-97-8 3,3-dimethyl-butan-2-one 

Downstream Products

• 38083-17-9 climbazole 

Relevant articles and documents

NOVEL NEISSERIA MENINGITIDIS SEROGROUP Y OLIGOMER AND PROCESS FOR SYNTHESIZING THEREOF

The present invention relates to novel oligomers of Neisseria meningitidis serogroup Y capsular polysaccharide repeating unit (Men-Y oligomers) and process for synthesizing novel Men- Y oligomers. Inparticular, the present invention relates to the chemical synthesis of the tetramer of Men- Y capsular polysaccharide repeating unit capable of being used as a candidate in the development of semisynthetic or fully synthetic conjugate vaccine against meningococcal serogroup Y bacterial infection.

Preparation of 3,3-dimethyl-1-phenoxy-butan-2-ols as fungicide intermediates

3,3-Dimethyl-1-phenoxy-butan-2-ols of the formula STR1 in which Y is a halogen atom, an optionally substituted phenyl radical, an optionally substituted phenoxy radical or a nitro, cyano, alkyl, alkoxy, alkoxycarbonyl or cycloalkyl radical, and n is 0, 1, 2 or 3, exhibit plant growth stimulating properties and are also useful in the synthesis of known fungicides. They are produced from tert-butyloxirane and the corresponding phenols.

Antimicrobial agents and their use

The invention involves the provision of compositions containing a 3,3-dialkyl- or 3-aryl-phenoxy-1-(1,2,4-triazol-1-yl)- and (imidazol-1-yl-alkan-2-ol) ethers which are particularly effective as antimicrobial especially antimycotic, agents. The invention also includes use of said compositions for providing antimicrobial, particularly antimycotic effect.