112062-62-1

Upstream product

• 78056-39-0 4,5-difluoro-2-nitroaniline 
• 3863-11-4 3,4-difluoroaniline 
• 458-11-7 3,4-difluoroacetanilide 
• 1662-21-1 N-(3,4-difluoro-2-nitrophenyl)acetamide 

Downstream Products

• 1557037-07-6 4‐bromo‐5,6‐difluoro‐2,1,3‐benzothiadiazole 

Relevant academic research and scientific papers

Vinylene-bridged difluorobenzo[: C] [1,2,5]-thiadiazole (FBTzE): A new electron-deficient building block for high-performance semiconducting polymers in organic electronics

A new class of an acceptor unit, vinylene-bridged 5,6-difluorobenzothiadiazole FBTzE, has been developed. Palladium-catalyzed Migita-Kosugi-Stille coupling reactions of 1 with 2, yielding 3 and its sequential dehydrogenative coupling with 4, readily affor

IMIDAZOLE DERIVATIVES

Described herein are compounds of formula (I), The compounds of formula I act as DGAT1 inhibitors and can be useful in preventing, treating or acting as a remedial agent for hyperlipidemia, diabetes mellitus and obesity.

Glycine receptor antagonists and the use thereof

Methods of treating or preventing neuronal loss associated with stroke, ischemia, CNS trauma, hypoglycemia and surgery, as well as treating neurodegenerative diseases including Alzheimer's disease, amyotrophic lateral sclerosis, Huntington's disease and Down's syndrome, treating or preventing the adverse consequences of the hyperactivity of the excitatory amino acids, as well as treating anxiety, chronic pain, convulsions, inducing anesthesia and treating psychosis are disclosed by administering to an animal in need of such treatment a compound having high affinity for the glycine binding site, lacking PCP side effects and which crosses the blood brain barrier of the animal. Also disclosed are novel 1,4-dihydroquinoxaline-2,3-diones, and pharmaceutical compositions thereof. Also disclosed are highly soluble ammonium salts of 1,4-dihydroquinoxaline-2,3-diones.

Benzoylacetic acid ester derivatives and process for their preparations

The present invention is concerned with certain novel benzoylacetic acid ester derivatives (I) which are useful as a intermediates for synthesis of antibacterial agests. STR1 wherein R is a lower alkyl group, X is a halogen atom and Y is a chlorine or bro

Halogenobenzoic acid derivatives and their preparation

The present invention is concerned with certain novel halogenobenzoic acid derivatives of the following formula, STR1 wherein R is a chlorine atom, amino group or hydroxy group, X is a chlorine atom or bromine atom, which are useful intermediates for the

Process for the preparation of quinolonecarboxylic acid derivatives

The present invention is concerned with certain novel process for the preparation of quinolonecarboxylic acid derivatives of the following formula, wherein R1 is a lower alkyl group, X is a chlorine or bromine atom and Y is a halogen atom, which are usefu