736143-84-3

Basic information

• Product Name: (S)-4-methyl-1-phenyl-2-pentanol
• Synonyms: (S)-4-methyl-1-phenyl-2-pentanol
• CAS NO: 736143-84-3
• Molecular Weight: 178.274
• Mol File: 736143-84-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (S)-4-methyl-1-phenyl-2-pentanol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-methyl-1-phenyl-2-pentanol(736143-84-3)
• EPA Substance Registry System: (S)-4-methyl-1-phenyl-2-pentanol(736143-84-3)

Safety Data

• Hazardous Substances Data: 736143-84-3(Hazardous Substances Data)

Upstream product

• 17763-67-6 Phenyl triflate 
• 917-57-7 vinyllithium 
• 145429-22-7 2-isobutyl-5,5-dimethyl-1,3,2-dioxaborinane 
• 5349-62-2 4-Methyl-1-phenyl-2-pentanone 
• 300-57-2 allylbenzene 
• 920-39-8 isopropylmagnesium bromide 

Downstream Products

• 736144-04-0 ((S)-1-Hydroxymethyl-pentyl)-carbamic acid (S)-1-benzyl-3-methyl-butyl ester 
• 736143-86-5 (S)-2-((S)-1-Benzyl-3-methyl-butoxycarbonylamino)-hexanoic acid methyl ester 

Relevant articles and documents

Catalytic conjunctive cross-coupling enabled by metal-induced metallate rearrangement

Transition metal catalysis plays a central role in contemporary organic synthesis. Considering the tremendously broad array of transition metal-catalyzed transformations, it is remarkable that the underlying elementary reaction steps are relatively few in

Preparation of enantiomerically enriched flavor and fragrance components

The present invention includes a process for enantioselective preparation of a non-racemic compound, which is either usable as a fragrance or flavor component or is convertible to a fragrance or flavor component by one or more additional reaction steps. T