63762-81-2

Usage

Structure

A derivative of benzene with a fluorine atom, a methoxy group, a methyl group, and a nitro group.

Applications

Commonly used in the synthesis of other organic compounds and in the pharmaceutical industry.

Chemical properties

Useful intermediate in the production of various chemicals and pharmaceuticals.

Versatility

Presence of fluorine, methoxy, methyl, and nitro groups provides a range of diverse properties.

Industrial applications

Utilized in pharmaceuticals, agrochemicals, and materials science.

Upstream product

• 63762-78-7 1-fluoro-2-methoxy-4-methylbenzene 
• 63762-80-1 2-nitro-4-fluoro-5-hydroxy-toluene 
• 74-88-4 methyl iodide 
• 179816-26-3 3-hydroxy-2-fluoronitrobenzene 
• 38512-82-2 3-methoxy-4-nitrotoluene 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 63762-82-3 [(E)-2-(4-Fluoro-5-methoxy-2-nitro-phenyl)-vinyl]-dimethyl-amine 
• 71288-91-0 1,5-Difluoro-2-methoxy-4-methyl-benzene 
• 1263299-46-2 5-fluoro-4-methoxy-2-methylaniline 
• 1263299-47-3 tert-Butyl (5-fluoro-4-methoxy-2-methylphenyl)carbamate 

Relevant academic research and scientific papers

THIAZOLIDINONE COMPOUNDS AND USE THEREOF

A pharmaceutical composition containing a compound of Formula (I) for treating an opioid receptor-associated condition. Also disclosed is a method for treating an opioid receptor-associated condition using such a compound. Further disclosed are two sets of thiazolidinone compounds of formula (I): (i) compounds each having an enantiomeric excess greater than 90% and (ii) compounds each being substituted with deuterium.

Synthesis and evaluation of the antiovulatory activity of a variety of melatonin analogues

A series of melatonin analogues was synthesized and examined for ovulation-blocking activity. Deviation from the 5-methoxy group or substitution of the 1 position prevented activity. Activity was not particularly sensitive to minor variations in the N-acyl group nor was it significantly altered by methylation of position 2 or the α-methylene; however, a pronounced enhancement resulted from halogenation of the 6 position.

Amides as ovulation inhibitors

N-[2-(5-methoxy-6-haloindol-3-yl)ethyl]amides are valuable, orally active, ovulation inhibitors.