80141-91-9

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
4-Fluoro-2-methylbenzyl alcohol is used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals for its ability to contribute to the development of new and effective products in these fields.
Used as a Solvent in Organic Synthesis:
4-Fluoro-2-methylbenzyl alcohol is utilized as a solvent in organic synthesis due to its mild antiseptic properties and its capacity to facilitate chemical reactions, making it a preferred choice for various laboratory and industrial processes.
Used in Fragrance Industry:
4-Fluoro-2-methylbenzyl alcohol is employed as a fragrance ingredient in perfumes and personal care products, capitalizing on its aromatic scent to enhance the appeal of these consumer goods.

InChI:InChI=1/C8H9FO/c1-6-4-8(9)3-2-7(6)5-10/h2-4,10H,5H2,1H3

Upstream product

• 321-21-1 4-fluoro-2-methylbenzoic acid 
• 174403-69-1 4-fluoro-2-methyl benzoic acid methyl ester 
• 452-63-1 2-Bromo-5-fluorotoluene 

Downstream Products

• 862539-91-1 1-(bromomethyl)-4-fluoro-2-methylbenzene 
• 174403-69-1 4-fluoro-2-methyl benzoic acid methyl ester 
• 63082-45-1 4-fluoro-2-methylbenzaldehyde 
• 147754-12-9 4-fluoro-2-methylbenzonitrile 

Relevant academic research and scientific papers

Catalytic Asymmetric (3 + 3) Cycloaddition of Oxyallyl Zwitterions with α-Diazomethylphosphonates

The unique structure of oxyallyls represents a significant challenge for their catalytic asymmetric applications. Herein, an unprecedented chiral imidodiphosphoric acid-catalytic enantioselective (3 + 3) cycloaddition between oxyallyl zwitterions generate

HISTONE DEMETHYLASE INHIBITORS

Provided herein are substituted pyrazolylpyridine, pyrazolylpyridazine, and pyrazolylpyrimidine derivative compounds and pharmaceutical compositions comprising said compounds. The subject compounds and compositions are useful for inhibition histone demethylase. Furthermore, the subject compounds and compositions are useful for the treatment of cancer, such as prostate cancer, breast cancer, bladder cancer, lung cancer and/or melanoma and the like.

PYRROLOY2,3-c¨PYRIDINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND USE

Provision of a compound having a superior proton pump action, which shows an antiulcer activity and the like after conversion to an in vivo proton pump inhibitor, a production method thereof and use thereof. A pyrrolo[2,3-c]pyridine compound represented by the formula: wherein each symbol is as defined in the specification.

1-(Cyclohexyl)-4-aryl-4-piperidinecarboxylic acid derivatives

Novel 1-(cyclohexyl)-4-aryl-4-piperidinecarboxylic acid derivatives, bearing in the 4-position of the cyclohexyl ring a cyano group and an aryl moiety, said compounds displaying useful antihistaminic properties.