1584137-33-6

Basic information

• Product Name: (S)-5-(4-methoxyphenyl)pentan-2-ol
• Synonyms: (S)-5-(4-methoxyphenyl)pentan-2-ol
• CAS NO: 1584137-33-6
• Molecular Weight: 194.274
• Mol File: 1584137-33-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-5-(4-methoxyphenyl)pentan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-5-(4-methoxyphenyl)pentan-2-ol(1584137-33-6)
• EPA Substance Registry System: (S)-5-(4-methoxyphenyl)pentan-2-ol(1584137-33-6)

Safety Data

• Hazardous Substances Data: 1584137-33-6(Hazardous Substances Data)

Upstream product

• 1584137-48-3 C₁₂H₁₈O₂ 
• 36278-54-3 2-(4-methoxyphenyl)ethylmagnesium bromide 
• 14425-64-0 4-methoxyphenethyl bromide 
• 768-60-5 4-methoxyphenylacetylen 
• 16088-62-3 (S)-Propylene oxide 
• 100-66-3 methoxybenzene 
• 103094-81-1 5-(4-methoxyphenyl)pentan-2-ol 
• 52244-70-9 4-(4-methoxyphenyl)butan-1-ol 
• 56047-51-9 4-(4-methoxyphenyl)butyraldehyde 
• 3153-44-4 4-(4-methoxy-phenyl)-4-oxo-butyric acid 
• 66265-99-4 5-(4-methoxyphenyl)pentan-2-one 

Downstream Products

• 103094-81-1 5-(4-methoxyphenyl)pentan-2-ol 

Relevant articles and documents

Preparation of Optically Enriched Secondary Alkyllithium and Alkylcopper Reagents—Synthesis of (?)-Lardolure and Siphonarienal

Optically enriched secondary alkyl iodides were converted into secondary alkyllithium and secondary alkylcopper compounds with very high retention of configuration. Quenching with various electrophiles, including chiral epoxides, provided a range of chira

Iron-catalyzed arene alkylation reactions with unactivated secondary alcohols

A simple, iron-based catalytic system allows for the inter- and intramolecular arylation of unactivated secondary alcohols. This transformation expands the substrate scope beyond the previously required activated alcohols and proceeds under mild reaction conditions, tolerating air and moisture. Furthermore, the use of an enantioenriched secondary alcohol provides an enantioenriched product for the intramolecular reaction, thereby offering a convenient approach to nonracemic products.