1260868-82-3

Basic information

• Product Name: (E)-tert-butyl (5-hydroxy-5-phenylpent-2-en-1-yl)carbonate
• CAS NO: 1260868-82-3
• Molecular Weight: 278.348
• Mol File: 1260868-82-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-tert-butyl (5-hydroxy-5-phenylpent-2-en-1-yl)carbonate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-tert-butyl (5-hydroxy-5-phenylpent-2-en-1-yl)carbonate(1260868-82-3)
• EPA Substance Registry System: (E)-tert-butyl (5-hydroxy-5-phenylpent-2-en-1-yl)carbonate(1260868-82-3)

Safety Data

• Hazardous Substances Data: 1260868-82-3(Hazardous Substances Data)

Upstream product

• 80735-94-0 1-Phenyl-3-buten-1-ol 
• 100-52-7 benzaldehyde 
• 115580-32-0 (Z)-but-2-ene-1,4-diyl di-tert-butyl dicarbonate 
• 24424-99-5 di-tert-butyl dicarbonate 

Relevant articles and documents

Stereoselective synthesis of 1,3-amino alcohols by the Pd-catalyzed cyclization of trichloroacetimidates

The synthesis of 4-vinyl-5,6-dihydro-1,3-oxazines, precursors of 1,3-amino alcohols, using the palladium-catalyzed cyclization of trichloroacetimidates is reported. The reaction favors the formation of the 4,6-cis-isomers with up to >20:1 diastereoselecti

Concise synthesis of tetrahydropyrans by a tandem oxa-michael/tsuji-trost reaction

A novel domino sequence facilitates the rapid assembly of polysubstituted tetrahydropyrans. The one-pot relay process generates up to three new stereogenic centers, including a tetrasubstituted carbon center, in a highly concise and convergent fashion from simple starting materials. Copyright