911689-29-7

Basic information

• Product Name: 3,5-dimethyl-5-phenylhex-1-yn-3-ol
• Synonyms: 3,5-dimethyl-5-phenylhex-1-yn-3-ol
• CAS NO: 911689-29-7
• Molecular Weight: 202.296
• Mol File: 911689-29-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,5-dimethyl-5-phenylhex-1-yn-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dimethyl-5-phenylhex-1-yn-3-ol(911689-29-7)
• EPA Substance Registry System: 3,5-dimethyl-5-phenylhex-1-yn-3-ol(911689-29-7)

Safety Data

• Hazardous Substances Data: 911689-29-7(Hazardous Substances Data)

Upstream product

• 7403-42-1 4-Methyl-4-phenyl-2-pentanone 
• 74-86-2 acetylene 

Downstream Products

• 728025-44-3 3-[2-(3,4-dimethoxyphenyl)ethyl]-4-hydroxy-4,5-dimethyl-5-(2-methyl-2-phenylpropyl)-1,3-oxazolidin-2-one 
• 727664-58-6 4-hydroxy-4,5-dimethyl-5-(2-methyl-2-phenylpropyl)-3-phenethyl-1,3-oxazolidin-2-one 
• 727664-59-7 3-benzyl-4-hydroxy-4,5-dimethyl-5-(2-methyl-2-phenylpropyl)-1,3-oxazolidin-2-one 
• 727663-49-2 3-ethyl-4-hydroxy-4,5-dimethyl-5-(2-methyl-2-phenylpropyl)-1,3-oxazolidin-2-one 
• 727663-93-6 4-hydroxy-3,4,5-trimethyl-5-(2-methyl-2-phenylpropyl)-1,3-oxazolidin-2-one 
• 727664-56-4 4-hydroxy-4,5-dimethyl-5-(2-methyl-2-phenylpropyl)-1,3-oxazolidin-2-one 

Relevant articles and documents

Synthesis of annulated oxazolidinones as potential precursors of cyclic cis-β-amino alcohols

A simple method for the synthesis of annulated 1,3-oxazolidin-2-ones from accessible ketones, acetylene, and carbon dioxide was developed. If their molecules contain arylalkyl substituents, intramolecular cyclization in acidic media gave rise to fused heterocyclic systems in high yields. The effects of the substituents in positions 3 and 5 of the oxazolidine ring on the regioselectivity of this cyclization were studied. The possibilities of converting oxazolidinones into cyclic cis-β-amino alcohols were studied.