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Usage

Uses

Used in Fragrance Industry:
1-(3-chloro-4-methylphenyl)ethanone is used as a fragrance ingredient for its sweet, floral scent, adding depth and complexity to perfumes and cosmetics.
Used in Pharmaceutical Industry:
As an intermediate in the synthesis of pharmaceuticals, 1-(3-chloro-4-methylphenyl)ethanone plays a crucial role in the development of various medicinal compounds, contributing to the advancement of healthcare solutions.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 1-(3-chloro-4-methylphenyl)ethanone serves as an intermediate, facilitating the creation of products that support agricultural practices and crop protection.
Used in Organic Synthesis:
1-(3-chloro-4-methylphenyl)ethanone is used as a precursor in the preparation of other organic compounds, showcasing its utility in expanding the range of synthetic possibilities in organic chemistry.
Used in Antimicrobial Applications:
It has been studied for its potential antimicrobial properties, indicating that 1-(3-chloro-4-methylphenyl)ethanone could be utilized as an antimicrobial agent in various applications where control of microbial growth is necessary.

Upstream product

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

Downstream Products

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

Relevant academic research and scientific papers

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.

2-Fluorobenzenesulfonyl compounds for the treatment of inflammation

Methods of treating cyclooxygenase-2 mediated disorders comprising administering to a subject a therapeutically effective amount of one or more 2-fluorobenzenesulfonyl compounds corresponding to Formula I: wherein A, R1, R2, and R3 are as described in the specification, and novel 2 fluorobenzenesulfonyl compounds within Formula I.

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.