1346155-37-0

Basic information

• Product Name: 4-methyl-1-phenylpent-1-yn-3-yl benzoate
• Synonyms: 4-methyl-1-phenylpent-1-yn-3-yl benzoate
• CAS NO: 1346155-37-0
• Molecular Weight: 278.351
• Mol File: 1346155-37-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-methyl-1-phenylpent-1-yn-3-yl benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-1-phenylpent-1-yn-3-yl benzoate(1346155-37-0)
• EPA Substance Registry System: 4-methyl-1-phenylpent-1-yn-3-yl benzoate(1346155-37-0)

Safety Data

• Hazardous Substances Data: 1346155-37-0(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 
• 139313-56-7 4-methyl-1-phenyl-pent-1-yn-3-ol 
• 98-88-4 benzoyl chloride 

Downstream Products

• 1346155-65-4 1-isopropyl-1H-inden-3-yl benzoate 
• 55033-17-5 2-(benzoyloxy)-3-methylbutanoic acid 
• 65-85-0 benzoic acid 
• 126518-76-1 1-methoxy-3-methyl-1-oxobutan-2-yl-benzoate 

Relevant articles and documents

Camphor-based Schiff base ligand SBAIB: An enantioselective catalyst for addition of phenylacetylene to aldehydes

A series of Schiff base ligands were synthesized from (1R)-camphor. Under the optimal conditions, (+)-SBAIB-a, 10 was found to be an excellent catalyst for the enantioselective addition of phenylacetylene to various aldehydes without utilizing either achiral additives or Ti(OiPr)4. This approach yielded (R)-propargylic alcohols in extremely high yields (up to 99%) and excellent enantioselectivities (up to 92%). The corresponding (S)-propargylic alcohols were synthesized in good to high enantioselectivities (up to 91%) and excellent yields (up to 99%) using (-)-SBAIB-a, 41.