122410-19-9

Basic information

• Product Name: 5-(4-Methoxyphenyl)-2-methylpent-1-en-3-ol
• Synonyms: 5-(4-Methoxyphenyl)-2-methylpent-1-en-3-ol
• CAS NO: 122410-19-9
• Molecular Weight: 206.285
• Mol File: 122410-19-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 5-(4-Methoxyphenyl)-2-methylpent-1-en-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-Methoxyphenyl)-2-methylpent-1-en-3-ol(122410-19-9)
• EPA Substance Registry System: 5-(4-Methoxyphenyl)-2-methylpent-1-en-3-ol(122410-19-9)

Safety Data

• Hazardous Substances Data: 122410-19-9(Hazardous Substances Data)

Upstream product

• 870-63-3 prenyl bromide 
• 114423-21-1 (+/-)-3-(4-methoxyphenylethyl)-2,2-dimethyloxirane 
• 824-94-2 p-methoxybenzyl chloride 
• 4586-91-8 1-methoxy-4-(4-methylpent-3-en-1-yl)benzene 
• 1332285-12-7 (S)-5-(4-methoxyphenyl)-2-methylpentane-2,3-diol 
• 1332285-28-5 (S)-3-(4-methoxyphenylethyl)-2,2-dimethyloxirane 
• 1332285-13-8 (R)-3-(4-methoxyphenylethyl)-2,2-dimethyloxirane 
• 20401-88-1 3-(4-methoxyphenyl)propional 
• 13291-18-4 isopropenylmagnesium bromide 
• 557-93-7 2-bromoprop-1-ene 

Downstream Products

• 129150-17-0 (E)-7-(4-Methoxy-phenyl)-4-methyl-hept-4-enoic acid ethyl ester 
• 1402736-05-3 (E)-2-(6-(4-methoxyphenyl)-3-methylhex-3-en-1-yl)-1,3-dioxane 
• 129150-04-5 (E)-1-<8,8-(1,2-Benzenediyldithio)-4-methylocta-3,7-dienyl>-4-methoxybenzene 
• 129150-03-4 (E)-7-(4-Methoxyphenyl)-4-methylhept-4-en-1-al 
• 129150-18-1 (E)-7-(4-methoxyphenyl)-4-methylhept-4-en-1-ol 
• 122410-12-2 1-Methoxy-4-(4-methyl-3-phenylsulfanylmethoxy-pent-4-enyl)-benzene 

Relevant articles and documents

Asymmetric syntheses of 8-oxabicyclo[3,2,1]octanes: A cationic cascade cyclization

High octane: A novel and practical syntheses of 8-oxabicyclo[3.2.1]octanes using a cationic cascade cyclization reaction has been developed (see scheme; TIPS=triisopropylsilyl). The diastereomer of the cyclization product isolated depends upon whether the acetal or aldehyde substrate is used. Copyright

Enantioselective Cationic Polyene Cyclization vs Enantioselective Intramolecular Carbonyl-Ene Reaction

This paper describes highly efficient catalytic enantioselective cationic polyene cyclization and catalytic enantioselective intramolecular carbonyl-ene reaction in good to high yields with high enantioselectivities. The intimate relationship and mechanistic differences between the two enantioselective reactions were studied in detail. In addition, the cyclization products are versatile and useful building blocks for natural products and pharmaceuticals syntheses.