14659-60-0

Usage

Uses

Used in Flavoring Industry:
Benzoic acid, 4-fluoro-2,6-dimethyl-, methyl ester is used as a flavoring agent for its distinctive fruity scent, enhancing the taste and aroma of various foods and beverages.
Used in Fragrance Industry:
This ester is employed in the production of fragrances, capitalizing on its pleasant odor to create appealing scents for a range of consumer products.
Used in Pharmaceutical Industry:
Benzoic acid, 4-fluoro-2,6-dimethyl-, methyl ester serves as a precursor in the synthesis of pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Chemical Synthesis:
In the realm of chemical synthesis, this ester is utilized as an intermediate in the production of other organic compounds, showcasing its versatility in the chemical industry.

InChI:InChI=1/C10H11FO2/c1-6-4-8(11)5-7(2)9(6)10(12)13-3/h4-5H,1-3H3

Upstream product

• 186581-53-3 diazomethane 
• 16633-50-4 4-fluoro-2,6-dimethyl benzoic acid 
• 315-12-8 2,6-dimethyl-4-fluoro-1-nitro-benzene 
• 392-70-1 2,6-dimethyl-4-fluoroaniline 
• 124-38-9 carbon dioxide 
• 14659-58-6 2‐bromo‐5‐fluoro‐1,3‐dimethylbenzene 
• 74-88-4 methyl iodide 
• 79909-92-5 methyl 4-amino-2,6-dimethylbenzoate 
• 19023-45-1 3,5-dimethyl-4-nitro-benzoic acid amide 
• 16643-19-9 4-Fluoro-2,6-dimethylbenzamide 
• 14659-61-1 2,6-dimethyl-4-fluorobenzonitrile 
• 34761-82-5 3,5-dimethyl-4-nitroaniline 
• 3095-38-3 3,5-dimethyl-4-nitrobenzoic acid 

Downstream Products

• 16633-50-4 4-fluoro-2,6-dimethyl benzoic acid 

Relevant academic research and scientific papers

Synthesis and Characterization of Acridinium Dyes for Photoredox Catalysis

Photoredox catalysis is a rapidly evolving platform for synthetic methods development. The prominent use of acridinium salts as a sustainable option for photoredox catalysts has driven the development of more robust and synthetically useful versions based on this scaffold. However, more complicated syntheses, increased cost, and limited commercial availability have hindered the adoption of these catalysts by the greater synthetic community. By utilizing the direct conversion of a xanthylium salt into the corresponding acridinium as the key transformation, we present an efficient and scalable preparation of the most synthetically useful acridinium reported to date. This divergent strategy also enabled the preparation of a suite of novel acridinium dyes, allowing for a systematic investigation of substitution effects on their photophysical properties.

Milled Dry Ice as a C1 Source for the Carboxylation of Aryl Halides

The use of carbon dioxide as a C1 chemical feedstock remains an active field of research. Here we showcase the use of milled dry ice as a method to promote the availability of CO 2in a reaction solution, permitting practical synthesis of arylcarboxylic acids. Notably, the use of milled dry ice produces marked increases in yields relative to those obtained with gaseous CO 2, as previously reported in the literature.

PIPERAZINE DERIVATIVES USEFUL AS CCR5 ANTAGONISTS

The use is described of CCR5 antagonists of formula (I) or a pharmaceutically acceptable salt thereof, wherein: R is optionally substituted phenyl, pyridyl, thiophenyl or naphthyl; R 1 is hydrogen or alkyl; R 2 is substituted phenyl, substituted heteroary

Piperazine derivatives useful as CCR5 antagonists

The use of CCR5 antagonists of the formula or a pharmaceutically acceptable salt thereof, wherein R is optionally substituted phenyl, pyridyl, thiophenyl or naphthyl; R1is hydrogen or alkyl; R2is substituted phenyl, substituted heter