93249-44-6

Usage

Uses

Used in Flavoring Industry:
2-Fluoro-5-methylbenzaldehyde is used as a flavoring agent for its distinctive and sweet scent, enhancing the taste and aroma of various food and beverage products.
Used in Pharmaceutical Industry:
2-Fluoro-5-methylbenzaldehyde is utilized as a precursor in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and medicines.
Used in Pesticide Industry:
This chemical serves as a key component in the production of pesticides, leveraging its aromatic properties to create effective pest control solutions.
Used in Dye Industry:
2-Fluoro-5-methylbenzaldehyde is employed in the creation of dyes, where its aromatic nature contributes to the color and stability of the final product.
Used in Fragrance Industry:
2-Fluoro-5-methylbenzaldehyde is used as a fragrance ingredient for its unique and appealing scent, adding value to perfumes, cosmetics, and other scented products.
Safety Precautions:
It is crucial to handle 2-Fluoro-5-methylbenzaldehyde with care, as it can be harmful if it comes into contact with the skin or eyes. It should be stored in a cool, dry place away from direct sunlight to maintain its stability and effectiveness.

InChI:InChI=1/C8H7FO/c1-6-2-3-8(9)7(4-6)5-10/h2-5H,1H3

Upstream product

• 352-32-9 p-fluorotoluene 
• 4885-02-3 Dichloromethyl methyl ether 

Downstream Products

• 851753-68-9 4-(2-formyl-4-methyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester 
• 934691-75-5 5-methyl-2-(phenoxy)benzaldehyde 
• 869478-56-8 (S_S)-2-methyl-propane-2-sulfinic acid [(S)-2-methyl-1-(5-methyl-2-piperazin-1-yl-phenyl)-propyl]-amide 
• 869478-55-7 4-[2-((S)-1-amino-2-methyl-propyl)-4-methyl-phenyl]-piperazine-1-carboxylic acid tert-butyl ester 
• 869478-27-3 4-{4-methyl-2-[((S_S)-2-methyl-propane-2-sulfinylimino)-methyl]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester 
• 851484-99-6 4-{4-methyl-2-[(S)-2-methyl-1-((S_S)-2-methyl-propane-2-sulfinylamino)-propyl]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester 
• 869478-60-4 4-{4-methyl-2-[(S)-2-methyl-1-(2-methyl-propane-2-sulfonylamino)-propyl]-phenyl}-piperazine-1-carboxylic aicd tert-butyl ester 
• 869478-43-3 4-{4-methyl-2-[(S)-3-methyl-1-((S_S)-2-methyl-propane-2-sulfinylamino)-butyl]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester 
• 699016-43-8 tert-butyl [(2R)-2-(3-chlorophenyl)-2-hydroxyethyl][(1R)-2-[4-[(2-formyl-4-methylphenyl)thio]-phenyl]-1-methylethyl]carbamate 
• 1182350-28-2 [3-(2-formyl-4-methyl-phenoxy)-phenyl]-acetic acid ethyl ester 
• 1191415-61-8 S-(2-formyl-4-methylphenyl) ethanethioate 
• 1213237-53-6 2,2,2-trifluoro-N-(6-(2-fluoro-5-methylbenzoyl)imidazo[1,2-a]pyridin-2-yl)acetamide 
• 952568-49-9 (R)-tert-butyl 3-benzyl-4-(3-(2-(2-formyl-4-methylphenoxy)-5-methylphenyl)propanoyl)piperazine-1-carboxylate 

Relevant academic research and scientific papers

Direct formylation of fluorine-containing aromatics with dichloromethyl alkyl ethers

Formylations of fluorine-containing aromatic compounds with dichloromethyl alkyl ethers have been investigated. Dichloromethyl propyl ether and dichloromethyl butyl ether have been applied for the formylation of fluorine-containing anisoles to give the corresponding aldehydes in good yields. Application of these ethers is preferable to that of methyl ether, which is prepared from volatile methyl formate. Reaction of fluorine-containing phenols with these dichloromethyl alkyl ethers did not give salicylaldehyde derivatives, leading instead to corresponding aryl formates in high yields. A plausible mechanism is discussed.

Aminoguanidine hydrazone derivatives, process for producing the same and drugs thereof

The present invention is to provide a compound of the formula: wherein the ring A is an optionally substituted 5- to 6-membered aromatic heterocyclic ring, the ring B an optionally substituted 5- to 6-membered aromatic homocyclic ring or an optionally sub