27644-03-7

Basic information

• Product Name: Benzenemethanol, a-(3-methyl-2-butenyl)-
• CAS NO: 27644-03-7
• Molecular Formula: C12H16O
• Molecular Weight: 176.258
• Mol File: 27644-03-7.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, a-(3-methyl-2-butenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-(3-methyl-2-butenyl)-(27644-03-7)
• EPA Substance Registry System: Benzenemethanol, a-(3-methyl-2-butenyl)-(27644-03-7)

Safety Data

• Hazardous Substances Data: 27644-03-7(Hazardous Substances Data)

Upstream product

• 1171-49-9 benzoyl-triphenyl-silane 
• 870-63-3 prenyl bromide 
• 5908-41-8 benzoyltrimethylsilane 
• 26902-24-9 3-(benzyloxy)-3-methyl-1-butene 
• 129813-21-4 2-(1,1-dimethyl-2-propenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 100-52-7 benzaldehyde 
• 1207865-76-6 4-(4-methyl-1-phenylpent-3-enyloxy)but-2-ynyl pivalate 
• 503-60-6 3,3-dimethyl-allyl chloride 
• 25438-37-3 phenyl(trimethylsiloxy)acetonitrile 
• 35189-96-9 3-methyl-2-butenylmagnesium chloride 
• 58335-10-7 3-Methyl-2-butenylzinc bromide 
• 104-53-0 3-phenyl-propionaldehyde 
• 27644-02-6 2,2-dimethyl-1-phenylbut-3-en-1-ol 
• 123290-13-1 phenyltriisopropylsilylmethanone 

Downstream Products

• 25438-37-3 phenyl(trimethylsiloxy)acetonitrile 
• 61752-45-2 Z-1-phenylpent-3-en-1-one 
• 74157-93-0 trans-1-phenyl-3-penten-1-one 
• 4535-64-2 5-methyl-1-phenylhex-4-en-1-one 
• 4528-19-2 5-Methyl-1-phenyl-4-hexen-1-ol 
• 72486-22-7 4-Methyl-1-phenylpenta-1,3-diene 
• 69815-01-6 4-methyl-1-phenylpentane-1,4-diol 
• 54877-02-0 4-methyl-1-phenylpentane-1,3-diol 

Relevant articles and documents

Catalytic asymmetric aldehyde prenylation and application in the total synthesis of (-)-rosiridol and (-)-bifurcadiol

Chiral phosphoric acid-catalyzed asymmetric aldehyde prenylation has been established using an α,α-dimethyl allyl boronic ester. The transformation provides expedient access to a wide array of aryl, heteroaryl, aryl-substituted alkenyl and primary and sec

Highly regioselective and chemoselective titanocene mediated Barbier-type allylation reactions

Titanocene carboxylate 1 is an excellent chemoselective reagent for unprecedented α-regioselective Barbier-type reactions. It constitutes the first titanocene(iii) able to tolerate epoxides and readily reduced carbonyl compounds, such as aromatic and α,β-unsaturated aldehydes. The Royal Society of Chemistry.