1334880-63-5

Basic information

• Product Name: ethyl (1S,2S,5S)-2-(tert-butoxycarbonylamino)-5-fluorocyclohexanecarboxylate
• Synonyms: ethyl (1S,2S,5S)-2-(tert-butoxycarbonylamino)-5-fluorocyclohexanecarboxylate
• CAS NO: 1334880-63-5
• Molecular Weight: 289.347
• Mol File: 1334880-63-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl (1S,2S,5S)-2-(tert-butoxycarbonylamino)-5-fluorocyclohexanecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (1S,2S,5S)-2-(tert-butoxycarbonylamino)-5-fluorocyclohexanecarboxylate(1334880-63-5)
• EPA Substance Registry System: ethyl (1S,2S,5S)-2-(tert-butoxycarbonylamino)-5-fluorocyclohexanecarboxylate(1334880-63-5)

Safety Data

• Hazardous Substances Data: 1334880-63-5(Hazardous Substances Data)

Upstream product

• 20205-48-5 8-oxo-7-azabicyclo<4.2.0>oct-2-ene 
• 189125-29-9 (1R,2S)-cis-2-aminocyclohex-4-enecarboxylic acid 
• 1334880-42-0 tert-butyl (1R,2S,5S)-7-oxo-6-oxabicyclo[3.2.1]oct-3-en-2-ylcarbamate 
• 1334880-41-9 tert-butyl (1R,2S,4S,5S)-4-iodo-7-oxo-6-oxabicyclo[3.2.1]octan-2-ylcarbamate 
• 1226812-49-2 (1R,6S)-6-(tert-butoxycarbonylamino)cyclohex-3-enecarboxylic acid 
• 1228187-00-5 ethyl (1S,2S,5R)-2-(tert-butoxycarbonylamino)-5-hydroxycyclohexanecarboxylate 
• 1228186-99-9 ethyl (1S,2S,5S)-2-(tert-butoxycarbonylamino)-5-hydroxycyclohex-3-enecarboxylate 

Relevant articles and documents

Selective synthesis of new fluorinated alicyclic β-amino ester stereoisomers

New fluorinated alicyclic β-amino ester stereoisomers with a cyclohexene or cyclohexane skeleton were prepared from cis- or trans-2-aminocyclohex-3-enecarboxylic acids in five or six steps through a regio- and stereoselective hydroxylation and hydroxy-fluorine exchange. Fluorinated aminoester enantiomers were synthesized from enantiopure cis- or trans-2-aminocyclohexenecarboxylic acid (prepared byenzymatic resolution of the racemic substances). New fluorinated alicyclic β-amino ester stereoisomers with a cyclohexene or cyclohexane skeleton were prepared from cis-or trans-2-aminocyclohex-3-enecarboxylicacids in five or six steps. Copyright