6013-92-9

Basic information

• Product Name: Benzenemethanol, a-(1,1-dimethylethyl)-4-methoxy-
• CAS NO: 6013-92-9
• Molecular Formula: C12H18O2
• Molecular Weight: 194.274
• Mol File: 6013-92-9.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, a-(1,1-dimethylethyl)-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-(1,1-dimethylethyl)-4-methoxy-(6013-92-9)
• EPA Substance Registry System: Benzenemethanol, a-(1,1-dimethylethyl)-4-methoxy-(6013-92-9)

Safety Data

• Hazardous Substances Data: 6013-92-9(Hazardous Substances Data)

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 630-19-3 pivalaldehyde 
• 630-18-2 tert-butyl isocyanide 
• 123-11-5 4-methoxy-benzaldehyde 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 3282-30-2 pivaloyl chloride 
• 594-19-4 tert.-butyl lithium 
• 631873-94-4 1-[(tert-butyl-dimethyl-silanyloxy)-(4-methoxy-phenyl)-methyl]-1H-imidazole 
• 507-20-0 tertiary butyl chloride 
• 2040-26-8 1-(4-methoxyphenyl)-2,2-dimethyl-1-propanone 
• 677-22-5 tert-butylmagnesium chloride 

Downstream Products

• 26110-92-9 1-(2,2-dimethylpropyl)-4-methoxybenzene 
• 345941-79-9 meso-3,4-Bis(4-methoxyphenyl)-2,2,5,5-tetramethylhexan 
• 86439-85-2 DL-3,4-Bis(4-methoxyphenyl)-2,2,5,5-tetramethylhexan 
• 86439-85-2 C₂₄H₃₄O₂ 
• 123-11-5 4-methoxy-benzaldehyde 
• 120328-80-5 (R)-(+)-2,2-dimethyl-1-(p-methoxyphenyl)propanol 
• 61986-69-4 (-)-(S)-1-(4-methoxyphenyl)-2,2-dimethylpropan-1-ol 
• 102808-04-8 C₂₂H₃₀O₂ 
• 2040-26-8 1-(4-methoxyphenyl)-2,2-dimethyl-1-propanone 
• 100-09-4 4-methoxybenzoic acid 
• 938-16-9 2,2-dimethylpropiophenone 
• 586346-65-8 2,2-dimethyl-1-{4-(trifluoromethyl)phenyl}propan-1-one 
• 110327-07-6 3-(4'-methoxyphenyl)-2,2,4,4-tetramethylpentyl 4-toluenesulfonate 
• 110327-05-4 methyl 3-(4'-methoxyphenyl)-2,2,4,4-tetramethylpentanoate 

Relevant articles and documents

Hydrogen-bonded networks in 1-(4-methoxyphenyl)-2,2-dimethyl-propan-1-ol

The asymmetric unit of the title compound, C12H18O2, contains two independent mol-ecules. They differ only slightly in conformation but form completely different inter-molecular hydrogen-bonded arrays. One molecule exhibits disorder in the hydroxy group r

Arylboronic Acid Catalyzed C-Alkylation and Allylation Reactions Using Benzylic Alcohols

The arylboronic acid catalyzed dehydrative C-alkylation of 1,3-diketones and 1,3-ketoesters using secondary benzylic alcohols as the electrophile is reported, forming new C-C bonds (19 examples, up to 98% yield) with the release of water as the only byproduct. The process is also applicable to the allylation of benzylic alcohols using allyltrimethylsilane as the nucleophile (12 examples, up to 96% yield).

Forming tertiary organolithiums and organocuprates from nitrile precursors and their bimolecular reactions with carbon electrophiles to form quaternary carbon stereocenters

Unstabilized tertiary organolithium intermediates are conveniently generated by reductive decyanation of nitriles, and these reagents and their derived cuprates couple in useful yields with carbon- centered electrophiles (see example). Chiral tertiary org