80865-61-8

Basic information

• Product Name: Benzenemethanol, 2-methoxy-3-(1-methylethyl)-
• CAS NO: 80865-61-8
• Molecular Formula: C11H16O2
• Molecular Weight: 180.247
• Mol File: 80865-61-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 2-methoxy-3-(1-methylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-methoxy-3-(1-methylethyl)-(80865-61-8)
• EPA Substance Registry System: Benzenemethanol, 2-methoxy-3-(1-methylethyl)-(80865-61-8)

Safety Data

• Hazardous Substances Data: 80865-61-8(Hazardous Substances Data)

Upstream product

• 88-69-7 2-(1-methylethyl)phenol 
• 77-78-1 dimethyl sulfate 
• 4397-16-4 2-hydroxymethyl-6-isopropylphenol 
• 67372-96-7 3-isopropylsalicylaldehyde 
• 91969-75-4 3-isopropyl-2-methoxybenzaldehyde 
• 50-00-0 formaldehyd 
• 2944-47-0 o-isopropylanisole 

Downstream Products

• 80865-60-7 (E)-2-Acetyl-8-(3-isopropyl-2-methoxy-phenyl)-5-methyl-oct-5-enoic acid ethyl ester 
• 80865-63-0 2-(3-Isopropyl-2-methoxy-benzyl)-3-(1-methyl-cyclopropyl)-3-oxo-propionic acid methyl ester 
• 80865-64-1 3-(3-Isopropyl-2-methoxy-phenyl)-1-(1-methyl-cyclopropyl)-propan-1-one 
• 80865-65-2 3-(3-Isopropyl-2-methoxy-phenyl)-1-(1-methyl-cyclopropyl)-propan-1-ol 
• 80865-66-3 1-((E)-6-Bromo-4-methyl-hex-3-enyl)-3-isopropyl-2-methoxy-benzene 
• 73414-41-2 (+/-)-triptophenolide methyl ether 
• 263157-56-8 (E)-5-(3-Isopropyl-2-methoxy-phenyl)-5-methoxymethoxy-2-methyl-pent-2-en-1-ol 
• 263157-55-7 1-isopropyl-2-methoxy-3-methoxymethoxymethyl-benzene 
• 80865-62-9 1-(bromomethyl)-3-isopropyl-2-methoxybenzene 

Relevant articles and documents

Deconjugative α-Alkylation of Cyclohexenecarboxaldehydes: An Access to Diverse Terpenoids

A general and efficient method for the deconjugative α-alkylation of α,β-unsaturated aldehydes promoted by a synergistic effect between tBuOK and NaH, which considerably increases the reaction rate under mild conditions, is reported. The β,γ-unsaturated aldehyde, resulting from the α-alkylation, is transformed in high yield into the corresponding allyl acetate via a lead(IV) acetate-mediated oxidative fragmentation. This strategy could be used for the construction of the carbon skeleton of a wide variety of alkyl or arylterpenoids.

Biogenetic-type synthesis of (±)-triptonide and (±)-triptolide

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