17474-12-3

Basic information

• Product Name: Benzenemethanol, a-(3,3-dimethyl-1-butynyl)-
• Synonyms: 4,4-dimethyl-1-hydroxy-1-phenyl-2-pentyne;4,4-Dimethyl-1-phenyl-pent-2-yn-1-ol;1-phenyl-4,4-dimethyl-2-pentyn-1-ol;4,4-dimethyl-1-phenyl-2-pentyn-1-ol;4,4-dimethyl-1-phenylpent-2-yn-1-ol
• CAS NO: 17474-12-3
• Molecular Formula: C13H16O
• Molecular Weight: 188.269
• Mol File: 17474-12-3.mol
• Article Data: 23

Chemical Properties

• Boiling Point: 73 - 75 °C (0.001 mmHg)
• Density: 1.010±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzenemethanol, a-(3,3-dimethyl-1-butynyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-(3,3-dimethyl-1-butynyl)-(17474-12-3)
• EPA Substance Registry System: Benzenemethanol, a-(3,3-dimethyl-1-butynyl)-(17474-12-3)

Safety Data

• Hazardous Substances Data: 17474-12-3(Hazardous Substances Data)

Upstream product

• 917-92-0 3,3-Dimethylbut-1-yne 
• 100-52-7 benzaldehyde 
• 66530-03-8 (3,3-dimethylbut-1-ynyl)dimethylaluminium 
• 104480-60-6 (3,3-dimethylbut-1-yn-1-yl)magnesium bromide 
• 23700-63-2 1-iodo-3,3-dimethylbut-1-yne 
• 62276-26-0 B-1-(3,3-dimethylbutynyl)-9-borabicyclo<3.3.1>nonane 
• 110-82-7 cyclohexane 
• 17475-11-5 1-phenyl-4,4-dimethylpent-2-yn-1-one 

Downstream Products

• 17475-11-5 1-phenyl-4,4-dimethylpent-2-yn-1-one 
• 866562-21-2 4,4-dimethyl-1-phenylpent-2-ynyl acetate 
• 538-44-3 4,4-dimethyl-1-phenyl-1-penten-3-one 
• 1196968-51-0 C₂₂H₂₅NO₂ 
• 28435-47-4 (Z)-4,4-dimethyl-1-phenylpent-1-en-3-one 
• 538-44-3 (E)-benzylidenepinacolone 
• 203172-78-5 4,4-dimethyl-1-phenyl-2-pentyne 
• 1402611-23-7 benzyl (E)-(4,4-dimethyl-1-phenylpent-2-yn-1-ylidene)carbamate 
• 464925-01-7 (R)-4,4-dimethyl-1-phenyl-2-pentyn-1-ol 
• 1426146-73-7 (R)-4,4-dimethyl-1-phenylpent-2-ynyl acetate 
• 16301-90-9 1-(diphenylphosphoryl)-4,4-dimethyl-1-phenylpentan-3-one 

Relevant articles and documents

Propargylation of CoQ0 through the Redox Chain Reaction

An efficient catalytic propargylation of CoQ0 is described by employing the cooperative effect of Sc(OTf)3 and Hantzsch ester. It is suggested to work through the redox chain reaction, which involves hydroquinone and dimeric propargylic moiety intermediates. A broad range of propargylic alcohols can be converted into the appropriate derivatives of CoQ0 containing triple bonds in good to excellent yields. The mechanism of the given transformation is also discussed.

Regioselective Rh-Catalyzed Hydroformylation of 1,1,3-Trisubstituted Allenes Using BisDiazaPhos Ligand

The efficient hydroformylation of 1,1,3-trisubstituted allenes is accomplished with low loadings of a Rh catalyst supported by a BisDiazaPhos (BDP) ligand. The ligand identity is key to achieving high regioselectivity, while the mild reaction conditions m

Redox-Neutral Arylations of Vinyl Cation Intermediates

Herein we present a new unified concept for C?C bond formation under redox-neutral conditions. Our strategy hinges upon interception of a vinyl cation with a sulfoxide resulting in simultaneous C–C and C?O bond formation and arylation. A range of structurally diverse vinyl cations are generated in situ in the presence of a sulfoxide, resulting in hydrative arylation, direct arylation of enol triflates and interrupted Meyer–Schuster rearrangement. Mechanistic investigations showcase the crucial role played by the fleeting vinyl cation intermediate and structural features that lead to its stabilization. Applications of the reaction products to synthesis are also presented. (Figure presented.).