374716-64-0

Basic information

• Product Name: 1-Propanol, 3-[(4-methoxyphenyl)methoxy]-2-methyl-
• CAS NO: 374716-64-0
• Molecular Formula: C12H18O3
• Molecular Weight: 210.273
• Mol File: 374716-64-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Propanol, 3-[(4-methoxyphenyl)methoxy]-2-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanol, 3-[(4-methoxyphenyl)methoxy]-2-methyl-(374716-64-0)
• EPA Substance Registry System: 1-Propanol, 3-[(4-methoxyphenyl)methoxy]-2-methyl-(374716-64-0)

Safety Data

• Hazardous Substances Data: 374716-64-0(Hazardous Substances Data)

Upstream product

• 2163-42-0 2-methyl-1.3-propanediol 
• 824-94-2 p-methoxybenzyl chloride 
• 2746-25-0 p-Methoxybenzyl bromide 

Downstream Products

• 374716-88-8 (R)-1-benzyloxy-3-(4-methoxybenzyloxy)-2-methylpropane 
• 136320-64-4 (2R)-3-[(4-methoxybenzyl)oxy]-2-methylpropanol 
• 160238-45-9 (2S)-3-(4-methoxybenzyloxy)-2-methyl-1-propanol 
• 374716-67-3 (S)-3-(4-methoxybenzyloxy)-2-methylpropyl acetate 
• 374716-65-1 (R)-3-(4-methoxybenzyloxy)-2-methylpropyl acetate 
• 443284-71-7 1-Methoxy-4-((Z)-(R)-2-methyl-non-3-enyloxymethyl)-benzene 
• 160238-46-0 (2R)-3-(4-methoxybenzyloxy)-2-methyl-1-propanal 
• 132969-60-9 (2S)-3-[(4-methoxybenzyl)oxy]-2-methylpropanal 

Relevant articles and documents

Photochemical Alkene Isomerization for the Synthesis of Polysubstituted Furans and Pyrroles under Neutral Conditions

A photochemical approach to polysubstituted heterocycles using UV-induced alkene isomerization is described. The method allows for the synthesis of disubstituted furans and pyrroles under mild and neutral conditions and also provides access to a class of trisubstituted furans pertinent to natural-product synthesis. The method has broad functional-group tolerance and many richly decorated heterocycles have been prepared incorporating functional groups that are unstable under Br?nsted and Lewis acidic conditions.

Synthesis of (+)-discodermolide by catalytic stereoselective borylation reactions

The marine natural product (+)-discodermolide was first isolated in 1990 and, to this day, remains a compelling synthesis target. Not only does the compound possess fascinating biological activity, but it also presents an opportunity to test current methods for chemical synthesis and provides an inspiration for new reaction development. A new synthesis of discodermolide employs a previously undisclosed stereoselective catalytic diene hydroboration and also establishes a strategy for the alkylation of chiral enolates. Furthermore, this synthesis of discodermolide provides the first examples of the asymmetric 1,4-diboration of dienes and borylative diene-aldehyde couplings in complex-molecule synthesis. Borylation-based synthesis: The development of a strategy for stereocontrol in catalytic diene hydroboration enables the synthesis of a critical building block for the assembly of (+)-discodermolide. Combined with asymmetric catalytic diboration, hydroformylation, and borylative aldehyde-diene coupling reactions, (+)-discodermolide could then be prepared from simple hydrocarbon-based building blocks.

Novel chiral lipoxygenase substrates: Design and synthesis. Part 2

A series of novel lipoxygenase substrates carrying a spacing modifier with a non-ionic hydroxyl terminus have been synthesized in an enantioselective fashion. One of the methylene hydrogens (flanked by the cis,cis-pentadienyl moiety) is replaced by alkyl,