1332954-73-0

Basic information

• Product Name: (E)-6-(p-tolyl)hex-3-en-1-ol
• Synonyms: (E)-6-(p-tolyl)hex-3-en-1-ol
• CAS NO: 1332954-73-0
• Molecular Weight: 190.285
• Mol File: 1332954-73-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-6-(p-tolyl)hex-3-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-6-(p-tolyl)hex-3-en-1-ol(1332954-73-0)
• EPA Substance Registry System: (E)-6-(p-tolyl)hex-3-en-1-ol(1332954-73-0)

Safety Data

• Hazardous Substances Data: 1332954-73-0(Hazardous Substances Data)

Upstream product

• 81036-83-1 4-(p-tolyl)butanal 
• 24306-23-8 methyl 4-(4-methylphenyl)butanoate 
• 4521-22-6 4-(4-methylphenyl)butyric acid 
• 4619-20-9 3-(4-methylbenzoyl)propionic acid 
• 22557-04-6 1-(but-3-yn-1-yl)-4-methylbenzene 
• 1332955-36-8 6-(p-tolyl)hex-3-yn-1-ol 

Downstream Products

• 1353372-71-0 C₂₀H₂₄O₃S 
• 1332955-41-5 C₁₃H₁₇N₃ 
• 1332955-17-5 (E)-6-(p-tolyl)hex-3-ene-1-thiol 
• 1332954-95-6 (E)-4-methyl-N-(6-p-tolylhex-3-enyl)benzenesulfonamide 
• 1332955-51-7 C₁₅H₂₀OS 
• 1332955-45-9 C₁₃H₁₉N 

Relevant articles and documents

Metal-Free Enantioselective Oxidative Arylation of Alkenes: Hypervalent-Iodine-Promoted Oxidative C?C Bond Formation

The enantioselective oxyarylation of (E)-6-aryl-1-silyloxylhex-3-ene was achieved using a lactate-based chiral hypervalent iodine(III) reagent in the presence of boron trifluoride diethyl etherate. The silyl ether promotes the oxidative cyclization, and enhances the enantioselectivity. In addition, the corresponding aminoarylation was achieved.