122427-58-1

Basic information

• Product Name: 4-(2'-methoxy-4'-methylphenyl)-n-pentyldimethylcarbinol
• Synonyms: 4-(2'-methoxy-4'-methylphenyl)-n-pentyldimethylcarbinol
• CAS NO: 122427-58-1
• Molecular Weight: 250.381
• Mol File: 122427-58-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-(2'-methoxy-4'-methylphenyl)-n-pentyldimethylcarbinol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2'-methoxy-4'-methylphenyl)-n-pentyldimethylcarbinol(122427-58-1)
• EPA Substance Registry System: 4-(2'-methoxy-4'-methylphenyl)-n-pentyldimethylcarbinol(122427-58-1)

Safety Data

• Hazardous Substances Data: 122427-58-1(Hazardous Substances Data)

Upstream product

• 917-64-6 methyl magnesium iodide 
• 76337-12-7 methyl 5-(2'-methoxy-4'-methylphenyl)hexanoate 
• 74-88-4 methyl iodide 
• 108-55-4 glutaric anhydride, 
• 63023-50-7 methyl 5-(2-hydroxy-4-methylphenyl)-5-oxopentanoate 
• 29207-19-0 methyl 5-(2-methoxy-4-methylphenyl)-5-oxopentanoate 
• 4642-35-7 5-(2-hydroxy-4-methylphenyl)-5-oxopentanoic acid 
• 122427-55-8 5-(2'-methoxy-4'-methylphenyl)hexanoic acid 
• 1257259-78-1 2-(2-methoxy-4-methylphenyl)but-3-en-2-ol 
• 1257259-82-7 ethyl 5-(2-methoxy-4-methylphenyl)hex-4-enoate 
• 35633-35-3 2-methoxy-4-methylacetophenone 
• 71841-61-7 ethyl 5-(4-methyl-2-methoxylphenyl)hexanoate 
• 76337-10-5 5-(2'-methoxy-4'-methylphenyl)hex-2-enoic acid 
• 76337-09-2 3-(2'-methoxy-4'-methylphenyl)butanal 

Downstream Products

• 66879-51-4 2-methoxy-4-methyl-1-(6-methylhept-5-en-2-yl)benzene 
• 71306-08-6 8-Methoxycalamenene 

Relevant articles and documents

Facile syntheses of (±)-curcuphenol-(±)-curcudiol-±)- curcuhydroquinone, and (±)-curcuquinone

The syntheses of (±)-curcuphenol 1, (±)-curcudiol 2, (±)-curcuhydroquinone 3, and (±)-curcuquinone 4 have been achieved. The key steps involved in the syntheses were the Reformatsky reaction and hydrogenation reaction. Copyright

Syntheses of (±)-curcuphenol, (±)-curcudiol and (±)-curcuhydroquinone: A Johnson-Claisen rearrangement approach

The synthesis of (±)-curcuphenol 1, (±)-curcudiol 2, (±)-curcuhydroquinone 3 and (±)-curcuquinone 4 had been achieved, in which the Johnson-Claisen rearrangement was used as key step.

Studies in Terpenoids : Part XLVIII - Synthesis of 8-Methoxycalamene, a Sesquiterpene of Marine Origin

The known 3-(2'-methoxy-4'-methylphenyl)butanol (IIIb) has been elaborated to 4-(2'-methoxy-4'-methylphenyl)-n-pentyldimethylcarbinol (IV) via the intermediates (IIIc-IIIf).While treatment of the carbinol (IV) with polyphosphoric acid gives directly 8-met