197522-46-6

Basic information

• Product Name: (Z)-3-methyl-5-phenyl-2-pentene-1,5-diol
• Synonyms: (Z)-3-methyl-5-phenyl-2-pentene-1,5-diol
• CAS NO: 197522-46-6
• Molecular Weight: 192.258
• Mol File: 197522-46-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (Z)-3-methyl-5-phenyl-2-pentene-1,5-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-3-methyl-5-phenyl-2-pentene-1,5-diol(197522-46-6)
• EPA Substance Registry System: (Z)-3-methyl-5-phenyl-2-pentene-1,5-diol(197522-46-6)

Safety Data

• Hazardous Substances Data: 197522-46-6(Hazardous Substances Data)

Upstream product

• 29643-79-6 4-methyl-6-phenyl-5,6-dihydro-2H-pyran-2-one 
• 141-78-6 ethyl acetate 
• 7437-61-8 2-methyl-3,4-epoxy-1-butene 
• 100-52-7 benzaldehyde 
• 1026158-68-8 2,2,5-trimethyl-7-phenyl-2,3,6,7-tetrahydro-[1,2]oxasilepine 
• 332188-10-0 [2,2-bis(phenylthio)ethyl]dimethyl(3-methyl-1-phenylbut-3-enyloxy)silane 
• 1027464-11-4 iodomethyl-dimethyl-(3-methyl-1-phenyl-but-3-enyloxy)-silane 
• 1027418-94-5 chloromethyl-dimethyl-(3-methyl-1-phenyl-but-3-enyloxy)-silane 
• 23092-23-1 3-methyl-1-phenylbut-3-en-1-ol 
• 19041-17-9 methyl 4-bromo-3-methylbut-2-enoate 

Relevant articles and documents

Biocatalyzed preparation of the optically enriched stereoisomers of 4-methyl-2-phenyl-tetrahydro-2H-pyran (Doremox)

The four stereoisomers of the rose oxide analogue Doremox were prepared in enantiomerically enriched form by enantiospecific bakers' yeast reduction of suitable derivatives and by lipase-mediated kinetic resolution of diol precursors.

Umpolung of vinyloxiranes: Regio- and stereoselectivity of the In/Pd-mediated allylation of carbonyl compounds

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