25801-53-0

Basic information

• Product Name: Phenol, 3-methoxy-2-(3-methyl-2-butenyl)-
• Synonyms: Phenol,3-methoxy-2-(3-methyl-2-butenyl);2-(3-methylbut-2-enyl)-3-methoxyphenol;3-methoxy-2-(3-methyl-2-butenyl)phenol;3-Methoxy-2-<3-methyl-but-2-enyl>-phenol;2-(3-methyl-2-butenyl)-3-methoxyphenol;2-isopentenyl-3-methoxyphenol
• CAS NO: 25801-53-0
• Molecular Formula: C12H16O2
• Molecular Weight: 192.25400
• Mol File: 25801-53-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 296.9±25.0 °C(Predicted)
• Density: 1.024±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Phenol, 3-methoxy-2-(3-methyl-2-butenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 3-methoxy-2-(3-methyl-2-butenyl)-(25801-53-0)
• EPA Substance Registry System: Phenol, 3-methoxy-2-(3-methyl-2-butenyl)-(25801-53-0)

Safety Data

• Hazardous Substances Data: 25801-53-0(Hazardous Substances Data)

Upstream product

• 150-19-6 O-methylresorcine 
• 78-79-5 isoprene 
• 34191-90-7 1-methoxy-3-(2-methylbut-3-yn-2-yloxy)benzene 
• 870-63-3 prenyl bromide 
• 30778-86-0 1-methoxy-3-tetrahydropyran-2-yloxybenzene 
• 340825-70-9 4-[2-(2-tetrahydropyranyloxy)-6-methoxyphenyl]-2-methylbut-2-ene 
• 100520-17-0 2-(3'-methyl-2'-butenyl)-3-methoxy-2-cyclohexen-1-one 
• 598-25-4 Dimethylallene 
• 34252-38-5 1-(1,1-Dimethyl-allyloxy)-3-methoxy-benzene 
• 115-18-4 2-methyl-3-buten-2-ol 

Downstream Products

• 1006054-39-2 C₁₅H₁₈O₄ 
• 144852-11-9 (+/-)-4-prenylpterocarpin 
• 203912-72-5 (Z)-1-acetoxy-4-(2-acetoxy-6-methoxyphenyl)-2-methylbut-2-ene 
• 203912-71-4 1-(2-acetoxy-6-methoxyphenyl)-3-methylbut-2-ene 

Relevant articles and documents

Synthesis and biological activity of the structural analogues of (-)-cabenegrin A-I

A series of phenylbutene and butanol derivatives (6a-j, 12, 13, 15, 17, 24b,c, 26, 27a,b) were prepared from the readily available resorcinol derivatives 2a-f and 7-hydroxy-chroman (18). The products were tested for inhibitory activity on the LPS-induced

Cyclooctane or Cyclohexane Annulations Based on Intramolecular Additions of Allylsilanes to Conjugated Dienones

The scope and limitations of alkenyl dienone cyclizations for the formation of fused cyclooctane or cyclohexane systems are described.

REGIOSPECIFIC ALKENYLATION OF PHENOLS BY 1,1-DIMETHYLALLENE PROMOTED BY PLATINUM CATALYSTS

1,1-Dimethylallene reacts with phenolic substrates in the presence of catalytic amounts of platinum(II) complexes.A regiospecific C-alkenylation takes place, affording o-isopentenylphenols and 2,2-dimethylchromans.Possible reaction mechanisms are also discussed.