1438394-24-1

Basic information

• Product Name: N-benzyl-1-oxo-N-(penta-3,4-dien-1-yl)indane-2-carboxamide
• Synonyms: N-benzyl-1-oxo-N-(penta-3,4-dien-1-yl)indane-2-carboxamide
• CAS NO: 1438394-24-1
• Molecular Weight: 331.414
• Mol File: 1438394-24-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-benzyl-1-oxo-N-(penta-3,4-dien-1-yl)indane-2-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-1-oxo-N-(penta-3,4-dien-1-yl)indane-2-carboxamide(1438394-24-1)
• EPA Substance Registry System: N-benzyl-1-oxo-N-(penta-3,4-dien-1-yl)indane-2-carboxamide(1438394-24-1)

Safety Data

• Hazardous Substances Data: 1438394-24-1(Hazardous Substances Data)

Upstream product

• 107301-61-1 N-benzyl-4-amino-1-butyne 
• 100-46-9 benzylamine 
• 22955-77-7 methyl 1-indanone-2-carboxylate 
• 1240792-17-9 C₁₂H₁₅N 
• 142301-75-5 N-(tert-butoxycarbonyl)-N-benzyl-4-amino-1-butyne 

Downstream Products

• 460365-08-6 4-(4-cyanophenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester 
• 1438394-44-5 (2R,4'S)-1'-benzyl-4'-[1-(4-bromophenyl)vinyl]-2'Hspiro[indene-2,3'-piperidine]-1,2'(3H)-dione 
• 162997-33-3 tert-butyl 4-(4-cyanophenyl)piperidine-1-carboxylate 
• 162997-34-4 4-(piperidin-4-yl)benzonitrile hydrochloride 
• 1438394-45-6 (2R,4'S)-1'-benzyl-4'-[1-(4-chlorophenyl)vinyl]-2'Hspiro[indene-2,3'-piperidine]-1,2'(3H)-dione 
• 1438394-46-7 (2R,4'S)-1'-benzyl-4'-[1-(3-nitrophenyl)vinyl]-2'Hspiro[indene-2,3'-piperidine]-1,2'(3H)-dione 
• 1438394-47-8 (2R,4'R)-1'-benzyl-4'-[1-(2-thienyl)vinyl]-2'H-spiro[indene-2,3'-piperidine]-1,2'(3H)-dione 
• 1438394-48-9 (2R,4'S)-1'-benzyl-4'-((E)-4-phenylbuta-1,3-dien-2-yl)spiro[indene-2,3'-piperidine]-1,2'(3H)-dione 
• 1438394-49-0 (2R,4'S)-1'-benzyl-4'-((Z)-4-phenylbuta-1,3-dien-2-yl)spiro[indene-2,3'-piperidine]-1,2'(3H)-dione 
• 1438394-50-3 (2R,4'S)-1'-benzyl-4'-((Z)-4-(4-methoxyphenyl)buta-1,3-dien-2-yl)spiro[indene-2,3'-piperidine]-1,2'(3H)-dione 

Relevant articles and documents

Enantio- and diastereoselective palladium catalysed arylative and vinylative allene carbocyclisation cascades

The enantioselective synthesis of heavily decorated spirolactams has been accomplished via an arylative or vinylative allene carbocyclisation cascade. Mediated by silver phosphate, a range of allene-linked pro-nucleophiles and aryl or vinyl iodides were reacted in the presence of catalytic Pd(OAc)2 and chiral bis(oxazoline) ligands to afford the spirolactam products in good yields and high enantio- and diastereoselectivities. The Royal Society of Chemistry 2013.