135865-77-9

Basic information

• Product Name: (S)-N-(tert-Butoxycarbonyl)-1-phenyl-3-butenylamine
• Synonyms: (S)-N-(tert-Butoxycarbonyl)-1-phenyl-3-butenylamine
• CAS NO: 135865-77-9
• Molecular Weight: 247.337
• Mol File: 135865-77-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (S)-N-(tert-Butoxycarbonyl)-1-phenyl-3-butenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-(tert-Butoxycarbonyl)-1-phenyl-3-butenylamine(135865-77-9)
• EPA Substance Registry System: (S)-N-(tert-Butoxycarbonyl)-1-phenyl-3-butenylamine(135865-77-9)

Safety Data

• Hazardous Substances Data: 135865-77-9(Hazardous Substances Data)

Upstream product

• 273749-15-8 benzaldimine-triethylborane complex 
• 100-47-0 benzonitrile 
• 24424-99-5 di-tert-butyl dicarbonate 
• 4383-23-7 (S)-1-phenylbut-3-en-1-amine 
• 130887-59-1 N-(2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosyl)-1(S)-amino-1-phenyl-3-butene 
• 130887-64-8 (S)-1-phenylbut-3-en-1-amine hydrochloride 

Downstream Products

• 1357361-01-3 6-(bromomethyl)-4-phenyl-1,3-oxazinan-2-one 
• 326477-54-7 6-phenyl-5,6-dihydro-2,4(1H,3H)-pyridinedione 
• 1449466-90-3 (S)-N-(t-butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-phenyl-butan-1-amine 
• 130887-64-8 (S)-1-phenylbut-3-en-1-amine hydrochloride 
• 357187-63-4 ((3Z,5E)-(S)-7-Bromo-1-phenyl-hepta-3,5-dienyl)-carbamic acid tert-butyl ester 
• 359644-06-7 ((3Z,5E)-(S)-7-Hydroxy-1-phenyl-hepta-3,5-dienyl)-carbamic acid tert-butyl ester 
• 357187-62-3 ((Z)-(S)-4-Iodo-1-phenyl-but-3-enyl)-carbamic acid tert-butyl ester 
• 135865-78-0 tert-butyl (1S)-3-oxo-1-phenylpropylcarbamate 
• 103365-47-5 (S)-3-(tert-butoxycarbonylamino)-3-phenylpropanoic acid 

Relevant articles and documents

New enolate-carbodiimide rearrangement in the concise synthesis of 6-amino-2,3-dihydro-4-pyridinones from homoallylamines

Three-step synthesis of 6-amino-2,3-dihydro-4-pyridinones from homoallylamines involving NBS-mediated cyclization of N-(3-butenyl)ureas to 6-(bromomethyl)-2-iminourethanes, dehydrohalogenation and a novel rearrangement as a key step has been developed. Th

A new method of synthesis of 6-substituted piperidine-2,4-diones from homoallylamines

Mono- and dihomoallylamines serve as convenient precursors for the preparation of 6-substituted piperidine-2,4-diones. This transformation is based, on the one hand, on a simple and well-known halocyclocarbamation reaction proceeding by the addition of a

(-)-Sparteine-mediated α-lithiation of N-Boc-N-(p-methoxyphenyl)benzylamine: Enantioselective syntheses of (S) and (R) mono-and disubstituted N-Boc-benzylamines

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