476687-78-2

Basic information

• Product Name: (E)-3-methyl-5-phenyl-2-pentene-1,5-diol
• Synonyms: (E)-3-methyl-5-phenyl-2-pentene-1,5-diol
• CAS NO: 476687-78-2
• Molecular Weight: 192.258
• Mol File: 476687-78-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-3-methyl-5-phenyl-2-pentene-1,5-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-methyl-5-phenyl-2-pentene-1,5-diol(476687-78-2)
• EPA Substance Registry System: (E)-3-methyl-5-phenyl-2-pentene-1,5-diol(476687-78-2)

Safety Data

• Hazardous Substances Data: 476687-78-2(Hazardous Substances Data)

Upstream product

• 39652-50-1 5-hydroxy-3-methyl-5-phenyl-pent-2-enoic acid methyl ester 
• 100-52-7 benzaldehyde 
• 78-79-5 isoprene 
• 19041-17-9 methyl 4-bromo-3-methylbut-2-enoate 

Downstream Products

• 1075200-35-9 (E)-3-methyl-5-phenylpent-2-ene-1,5-diol diacetate 
• 476688-17-2 (1R,3S)-3-methyl-1-phenylpentane-1,5-diol 
• 149713-23-5 (2S,2S)-4-methyl-2-phenyl-tetrahydro-2H-pyran 
• 149713-23-5 (2R,2S)-4-methyl-2-phenyl-tetrahydro-2H-pyran 
• 201145-41-7 (E)-5-hydroxy-3-methyl-5-phenyl-pent-2-enal 

Relevant articles and documents

Diastereoselective construction of functionalized homoallylic alcohols by Ni-catalyzed diboron-promoted coupling of dienes and aldehydes

The nickel-catalyzed reaction of carbonyls and dienes was accomplished in a regio- and stereoselective fashion employing a stoichiometric amount of bis(pinacolato)diboron. This reductive coupling furnishes an allyl boronic ester as the reaction product, a compound which was readily converted to the derived allylic alcohol by oxidative workup. Copyright