1284206-60-5

Basic information

• Product Name: tert-butyl [(1R)-1-phenylprop-2-en-1-yl]prop-2-yn-1-ylcarbamate
• Synonyms: tert-butyl [(1R)-1-phenylprop-2-en-1-yl]prop-2-yn-1-ylcarbamate
• CAS NO: 1284206-60-5
• Molecular Weight: 271.359
• Mol File: 1284206-60-5.mol

Chemical Properties

• CAS DataBase Reference: tert-butyl [(1R)-1-phenylprop-2-en-1-yl]prop-2-yn-1-ylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl [(1R)-1-phenylprop-2-en-1-yl]prop-2-yn-1-ylcarbamate(1284206-60-5)
• EPA Substance Registry System: tert-butyl [(1R)-1-phenylprop-2-en-1-yl]prop-2-yn-1-ylcarbamate(1284206-60-5)

Safety Data

• Hazardous Substances Data: 1284206-60-5(Hazardous Substances Data)

Upstream product

• 106-96-7 propargyl bromide 
• 158851-29-7 (+)-tert-butyl [(1R)-1-phenylprop-2-en-1-yl]imidocarbonate 

Downstream Products

• 1284206-93-4 tert-butyl (3R,3aR)-5-oxo-3-phenyl-3,3a,4,5-tetrahydro-1H-cyclopenta[c]pyrrole-2-carboxylate 

Relevant articles and documents

Bicyclic cyclopentenones via the combination of an iridium-catalyzed allylic substitution with a diastereoselective intramolecular pauson-khand reaction

Enantioselective syntheses of bicyclic cyclopentenones are described. Key steps are an iridium-catalyzed allylic substitution and an intramolecular diastereoselective Pauson-Khand reaction. The diastereoselectivity of the Pauson-Khand reaction was found t