844699-02-1

Basic information

• Product Name: tert-butyl (2S,5S,6S)-2-benzyloxymethyl-6-[(1E,3R)-3-hydroxynon-1-enyl]-1-azaspiro[4.5]decane-1-carboxylate
• Synonyms: tert-butyl (2S,5S,6S)-2-benzyloxymethyl-6-[(1E,3R)-3-hydroxynon-1-enyl]-1-azaspiro[4.5]decane-1-carboxylate
• CAS NO: 844699-02-1
• Molecular Weight: 499.734
• Mol File: 844699-02-1.mol

Chemical Properties

• CAS DataBase Reference: tert-butyl (2S,5S,6S)-2-benzyloxymethyl-6-[(1E,3R)-3-hydroxynon-1-enyl]-1-azaspiro[4.5]decane-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (2S,5S,6S)-2-benzyloxymethyl-6-[(1E,3R)-3-hydroxynon-1-enyl]-1-azaspiro[4.5]decane-1-carboxylate(844699-02-1)
• EPA Substance Registry System: tert-butyl (2S,5S,6S)-2-benzyloxymethyl-6-[(1E,3R)-3-hydroxynon-1-enyl]-1-azaspiro[4.5]decane-1-carboxylate(844699-02-1)

Safety Data

• Hazardous Substances Data: 844699-02-1(Hazardous Substances Data)

Upstream product

• 484061-49-6 tert-butyl (2S,5S,6S)-2-benzyloxymethyl-6-[(1E,3S/R)-3-hydroxynon-1-enyl]-1-azaspiro[4.5]decane-1-carboxylate 
• 484061-45-2 tert-butyl (1S)-[(9E,11E)-1-benzyloxymethyl-4-oxo-9,11-octadecadienyl]carbamate 
• 152500-21-5 (S)-5-benzyloxymetyl-1-tert-butoxycarbonyl-2-pyrrolidinone 
• 484061-47-4 tert-butyl (2S,5S,6S)-2-benzyloxymethyl-6-[(1E,3S/R)-3-(formyloxy)non-1-enyl]-1-azaspiro[4.5]decane-1-carboxylate 
• 484061-51-0 tert-butyl (2S,5S,6S)-2-benzyloxymethyl-6-[(1E)-3-oxonon-1-enyl]-1-azaspiro[4.5]decane-1-carboxylate 

Downstream Products

• 844698-99-3 (3R)-1-[(2S,5S,6S)-2-benzyloxymethyl-1-azaspiro[4.5]dec-6-yl]-3-nonanol 
• 844699-00-9 (3S,5S,7aS,11′S)-3-(benzyloxymethyl)-5-hexyldecahydro-1H-pyrrolo[1,2-j]quinoline 
• 844698-98-2 tert-butyl (2S,5S,6S)-2-benzyloxymethyl-6-[(3R)-3-hydroxynonyl]-1-azaspiro[4.5]decane-1-carboxylate 

Relevant articles and documents

Total synthesis of the tricyclic marine alkaloids (-)-lepadiformine, (+)-cylindricine C, and (-)-fasicularin via a common intermediate formed by formic acid-induced intramolecular conjugate azaspirocyclization

A very short and efficient enantioselective total synthesis of the tricyclic marine alkaloids (-)-lepadiformine (3), (+)-cylindricine C (1c), and (-)-fasicularin (4) has been developed utilizing the formyloxy 1-azaspiro[4.5]decane 5 as a common intermedia