257628-68-5

Basic information

• Product Name: N-(2-bromobenzylidene)butan-1-amine
• Synonyms: N-(2-bromobenzylidene)butan-1-amine
• CAS NO: 257628-68-5
• Molecular Weight: 240.143
• Mol File: 257628-68-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-(2-bromobenzylidene)butan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-bromobenzylidene)butan-1-amine(257628-68-5)
• EPA Substance Registry System: N-(2-bromobenzylidene)butan-1-amine(257628-68-5)

Safety Data

• Hazardous Substances Data: 257628-68-5(Hazardous Substances Data)

Upstream product

• 109-73-9 N-butylamine 
• 6630-33-7 ortho-bromobenzaldehyde 

Downstream Products

• 195611-52-0 diethyl 1-(N-butylamino)-2-bromobenzylphosphonate 
• 257628-69-6 (2-Butylbenzylidene)butylamine 
• 950523-94-1 1-bromo-2-(2-nitro-2-(4-fluorophenyl)-vinyl)-benzene 
• 889878-44-8 3-(2-bromo-phenyl)-4-(4-fluoro-phenyl)-1H-pyrrole-2-carboxylic acid ethyl ester 
• 889878-45-9 3-(2-bromo-phenyl)-4-(4-fluoro-phenyl)-1-isopropyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 889878-46-0 3-(2-bromo-phenyl)-4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 889878-47-1 3-(2-bromo-phenyl)-4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-1H-pyrrole-2-carboxylic acid 
• 889878-48-2 3-(2-bromo-phenyl)-4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-1H-pyrrole-2-carboxylic acid phenylamide 
• 889878-49-3 1-(4-fluoro-phenyl)-3-isopropyl-4-oxo-5-phenyl-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-2-carbaldehyde 
• 889878-50-6 1-(4-fluoro-phenyl)-2-hydroxymethyl-3-isopropyl-5-phenyl-3,5-dihydro-pyrrolo[2,3-c]quinolin-4-one 

Relevant articles and documents

Tunable Synthesis of α-Amino Boronic Esters from Available Aldehydes and Amines through Sequential One-Pot Dehydration and Copper-Catalyzed Borylacylation

Copper-catalyzed multicomponent borylacylation of imines with acid chlorides and bis(pinacolato)diboron was developed for the preparation of synthetically useful and pharmacologically relevant α-amino boronic acid derivatives. Starting from a range of acid chlorides and imines with aryl, heteroaryl, and alkyl substituents, most of these ligand-free reactions proceeded smoothly at room temperature in moderate to good yields. Furthermore, a facile and convenient one-pot, multistep access to the direct synthesis of α-amino boronic acid derivatives from available aldehydes and amines was also developed.

Regioselective Cu(I)-catalyzed tandem A3-coupling/ decarboxylative coupling to 3-amino-1,4-enynes

An efficient and novel copper-mediated protocol for the synthesis of 3-amino-1,4-enynes from glyoxylic acid, an amine, and an alkyne was developed. This new reaction involving two sequential C-C bond formations is air and moisture tolerant and proceeds via a tandem A3-coupling and a selective decarboxylative coupling.

COMPOUNDS FOR IMPROVING LEARNING AND MEMORY

The present invention provides a compound of Formula I: (I) and methods for improving memory in a subject by administering a therapeutically effective amount of the compound.