71787-60-5

Basic information

• Product Name: Benzenepropanol, a-(1,1-dimethyl-2-propenyl)-
• CAS NO: 71787-60-5
• Molecular Formula: C14H20O
• Molecular Weight: 204.312
• Mol File: 71787-60-5.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: Benzenepropanol, a-(1,1-dimethyl-2-propenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanol, a-(1,1-dimethyl-2-propenyl)-(71787-60-5)
• EPA Substance Registry System: Benzenepropanol, a-(1,1-dimethyl-2-propenyl)-(71787-60-5)

Safety Data

• Hazardous Substances Data: 71787-60-5(Hazardous Substances Data)

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 78-79-5 isoprene 
• 870-63-3 prenyl bromide 
• 113365-21-2 1,1-diphenyl-2,2-dimethyl-3-buten-1-ol 
• 141550-13-2 4,4,5,5-tetramethyl-2-(3-methylbut-2-enyl)-1,3,2-dioxaborolane 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 24509-88-4 2-methyl-3-buten-2-yl acetate 
• 115-18-4 2-methyl-3-buten-2-ol 
• 129813-21-4 2-(1,1-dimethyl-2-propenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 503-60-6 3,3-dimethyl-allyl chloride 
• 114067-34-4 (3-methyl-2-butenyl)trifluorosilane 
• 61209-24-3 (Z)-3-methyl-2-butenyltrichlorosilane 
• 17314-40-8 3-Methyl-2-butenyl-trimethylstannane 

Downstream Products

• 68705-88-4 6-methyl-1-phenyl-hept-5-en-3-ol 
• 1283068-44-9 4,4-dimethyl-1,6-diphenylhexan-3-ol 

Relevant articles and documents

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Cp2TiCl2-Catalyzed Photoredox Allylation of Aldehydes with Visible Light

A Barbier-type Cp2TiCl2-mediated (10 mol %) photoredox allylation of aldehydes under irradiation with visible light (blue light-emitting diodes (LEDs), 450 nm) and in the presence of an organic dye (3DPAFIPN, 5 mol %) with allylbromides is described.

Transition-metal-free reductive coupling of 1, 3-butadienes with aldehydes catalyzed by dibutyliodotin hydride

In this study, the Bu2SnIH-catalyzed direct coupling of 1, 3- dienes with aldehydes was developed. This reaction could be suitable for coupling without the use of transition-metal catalysts. Many types of aldehydes were applied to this reaction. The addition of MeOH promoted the catalytic cycle.