90792-98-6

Basic information

• Product Name: 1-(3-chloro-4-methylphenyl)ethanone
• Synonyms: 1-(3-Chloro-4-methylphenyl)ethanone; ethanone, 1-(3-chloro-4-methylphenyl)-
• CAS NO: 90792-98-6
• Molecular Formula: C₉H₉ClO
• Molecular Weight: 168.6202
• Mol File: 90792-98-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 260.9°C at 760 mmHg
• Flash Point: 126°C
• Density: 1.13g/cm³
• Vapor Pressure: 0.0119mmHg at 25°C
• Refractive Index: 1.528
• CAS DataBase Reference: 1-(3-chloro-4-methylphenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-chloro-4-methylphenyl)ethanone(90792-98-6)
• EPA Substance Registry System: 1-(3-chloro-4-methylphenyl)ethanone(90792-98-6)

Safety Data

• Hazardous Substances Data: 90792-98-6(Hazardous Substances Data)

Usage

General Description

1-(3-chloro-4-methylphenyl)ethanone, also known as 4-chloro-3-methylacetophenone, is a chemical compound with the molecular formula C9H9ClO. It is a pale yellow liquid with a sweet, floral odor and is commonly used as a fragrance ingredient in perfumes and cosmetics. Additionally, it is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential antimicrobial properties and as a precursor in the preparation of other organic compounds. The chemical structure of 1-(3-chloro-4-methylphenyl)ethanone contains a chlorine atom, a methyl group, and a phenyl ring, making it a versatile compound for various applications in the chemical industry.

Upstream product

• 17071-24-8 1-(3-amino-4-methylphenyl)ethanone 
• 431-03-8 dimethylglyoxal 
• 95-74-9 3-chloro-p-toluidine 
• 21423-81-4 3-chloro-4-methylbenzonitrile 
• 370874-64-9 2-Fluoro-4-Hydrazino-Benzenesulfonamide 
• 122-00-9 para-methylacetophenone 
• 5333-27-7 1-(4-methyl-3-nitro-phenyl)-ethanone 

Downstream Products

• 5162-82-3 3-chloro-4-methylbenzoic acid 
• 1132701-01-9 3-[3-bromo-5-(trifluoromethyl) phenyl]-1-(3-chloro-4-methylphenyl)-4,4,4-trifluoro-3-hydroxybutane-1-one 
• 105321-42-4 3-chloro-4-methyl-α-methylbenzylamine 
• 91801-13-7 (+/-)-2-Isopropylamino-1-<3-chlor-4-methyl-phenyl>-aethanol-(1) 
• 804428-09-9 3-Chlor-α-isopropylamino-4-methyl-acetophenon 
• 1095275-16-3 3-(3,5-bis(trifluoromethyl)phenyl)-1-(3-chloro-4-methylphenyl)-4,4,4-trifluoro-3-hydroxybutan-1-one 
• 115382-35-9 4-carboxy-3-chloroacetophenone 

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.

Triazine derivatives, a process for preparing the derivatives, and herbicides containing the derivatives as the effective component

A triazine derivative represented by the general formula: STR1 wherein R1 and R2 are each an alkyl group having 1 to 4 carbon atoms, and X1 and X2 are each a halogen atom, an alkyl group having 1 to 4 carbon atoms, an alkoxyl group having 1 to 4 carbon atoms, or an alkylthio group having 1 to 4 carbon atoms. This invention also provides a process for efficiently preparing said triazine derivative and a herbicide containing said triazine derivative as effective component.