153783-18-7

Basic information

• Product Name: Ethyl (S)-2-(tert-butoxycarbonylamino)-5-phenyl-5-oxopentanoate
• Synonyms: Ethyl (S)-2-(tert-butoxycarbonylamino)-5-phenyl-5-oxopentanoate
• CAS NO: 153783-18-7
• Molecular Weight: 335.4
• Mol File: 153783-18-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethyl (S)-2-(tert-butoxycarbonylamino)-5-phenyl-5-oxopentanoate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl (S)-2-(tert-butoxycarbonylamino)-5-phenyl-5-oxopentanoate(153783-18-7)
• EPA Substance Registry System: Ethyl (S)-2-(tert-butoxycarbonylamino)-5-phenyl-5-oxopentanoate(153783-18-7)

Safety Data

• Hazardous Substances Data: 153783-18-7(Hazardous Substances Data)

Upstream product

• 108-86-1 bromobenzene 
• 251924-83-1 1-tert-butyl 2-ethyl 5-oxopyrrolidine-1,2-dicarboxylate 
• 144978-35-8 (S)-ethyl N-tert-butoxycarbonylpyroglutamate 
• 100-58-3 phenylmagnesium bromide 

Downstream Products

• 13355-43-6 5-phenyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 6636-06-2 5-phenyl-1H-pyrrole-2-carboxylic acid 
• 158567-93-2 β-(S)-5-Ethoxycarbonyl-2-phenylpyrrolidine 
• 153783-23-4 (S)-5-Ethoxycarbonyl-2-phenyl-Δ¹-pyrroline 

Relevant articles and documents

Convenient synthesis of C-aza-2,3-dideoxynucleosides

l-Aryl-l,2,3,4-tetradeoxy-l,4-imino-D-pentitols 5 and 9f are easily synthesized from TV-Boc-L-pyroglutamate 1 via a successive procedure involving regioselective ring-opening, recyclization with dehydration, stereoselective reduction, and reduction of the

General method for the synthesis of 5-arylpyrrole-2-carboxylic acids

5-Arylpyrrole-2-carboxylic acids are prepared by DDQ oxidative aromatization of the corresponding ethyl 2-aryl-Δ1-pyrroline-5-carboxylate followed by basic hydrolysis.