14401-72-0

Basic information

• Product Name: 3',5'-Dichloroacetophenone
• Synonyms: 3',5'-DICHLOROACETOPHENONE;Methyl 3,5-dichlorophenyl ketone;1-(3,5-dichlorophenyl)ethan-1-one;1-Acetyl-3,5-dichlorobenzene;3',5'-Dichloroacetophenone≥ 98% (GC)
• CAS NO: 14401-72-0
• Molecular Formula: C₈H₆Cl₂O
• Molecular Weight: 189.04
• Product Categories: Aromatic Acetophenones & Derivatives (substituted);Adehydes, Acetals & Ketones;Chlorine Compounds
• Mol File: 14401-72-0.mol
• Article Data: 7

Chemical Properties

• Melting Point: 26 °C
• Boiling Point: 82°C 0,1mm
• Flash Point: 119 °C
• Appearance: /
• Density: 1.304g/cm³
• Refractive Index: 1.5630 to 1.5670
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3',5'-Dichloroacetophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 3',5'-Dichloroacetophenone(14401-72-0)
• EPA Substance Registry System: 3',5'-Dichloroacetophenone(14401-72-0)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39-25/26
• Hazardous Substances Data: 14401-72-0(Hazardous Substances Data)

Usage

Chemical Properties

Light yellow liquid

Upstream product

• 184970-30-7 2-(3,5-dichlorophenyl)-2-propanol 
• 51-36-5 3,5-dichlorobenzoic acid 
• 917-54-4 methyllithium 
• 431-03-8 dimethylglyoxal 
• 626-43-7 3,5-Dichloroaniline 
• 3032-81-3 3,5-dichloroiodobenzene 
• 108-24-7 acetic anhydride 
• 75-16-1 methylmagnesium bromide 
• 259796-12-8 3,5-dichloro-N-methoxy-N-methylbenzamide 
• 6575-00-4 3,5-dichlorobenzonitrile 
• 74-88-4 methyl iodide 
• 5780-37-0 (E)-acetaldoxime 
• 7757-83-7 sodium sulfite 
• 99-92-3 p-aminobenzophenone 

Downstream Products

• 154257-66-6 3-(3,5-dichlorophenyl)-1H-pyrazole 
• 154257-73-5 3-(3,5-dichlorophenyl)-4-chloro-1H-pyrazole 
• 84580-08-5 (S)-α-(3,5-dichlorophenyl)ethylamine (+)-10-camphorsulfonic acid salt 
• 139752-43-5 1-(3,5-dichlorophenyl)ethanone oxime 
• 1379297-25-2 C₉H₆Cl₂O₃ 
• 1092654-02-8 C₁₅H₁₀Cl₂O 
• 150251-18-6 (3,5-Dichloro-phenyl)-oxo-acetaldehyde 

Relevant articles and documents

Photoinduced Acetylation of Anilines under Aqueous and Catalyst-Free Conditions

A green and efficient visible-light induced functionalization of anilines under mild conditions has been reported. Utilizing nontoxic, cost-effective, and water-soluble diacetyl as photosensitizer and acetylating reagent, and water as the solvent, a variety of anilines were converted into the corresponding aryl ketones, iodides, and bromides. With advantages of environmentally friendly conditions, simple operation, broad substrate scope, and functional group tolerance, this reaction represents a valuable method in organic synthesis.

SUBSTITUTED PYRAZOLES, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF USE

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Fungicidal arylpyrazoles

The present invention relates to new derivatives of the family of 3-arylpyrazoles of formula (I), their methods of preparation, the compositions containing them and their utilization for the protection of plants against fungal diseases. STR1