125642-05-9

Basic information

• Product Name: Benzenepropanol, a-[1-(phenylmethylene)heptyl]-, (E)-
• CAS NO: 125642-05-9
• Molecular Formula: C23H30O
• Molecular Weight: 322.491
• Mol File: 125642-05-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzenepropanol, a-[1-(phenylmethylene)heptyl]-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanol, a-[1-(phenylmethylene)heptyl]-, (E)-(125642-05-9)
• EPA Substance Registry System: Benzenepropanol, a-[1-(phenylmethylene)heptyl]-, (E)-(125642-05-9)

Safety Data

• Hazardous Substances Data: 125642-05-9(Hazardous Substances Data)

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 16967-02-5 1-phenyl-1-octyne 

Relevant articles and documents

Reactions between Tantalum- or Niobium-Alkyne Complexes and Carbonyl Compounds

A variety of tantalum-alkyne complexes are generated in situ by treatment of alkynes with low-valent tantalum derived from TaCl5 and zinc.These complexes add regioselectively to carbonyl compounds in a one-to-one fashion to yield (E)-allylic alcohols stereoselectively.Iodinolysis of the oxatantalacyclopentene, which is postulated as an intermediate of the reaction, gives a (Z)-3-iodo-2-propen-1-ol derivative.In contrast to tantalum-alkyne complexes, niobium-alkyne complexes, prepared with low-valent niobium derived from NbCl5 and zinc, add in situ to aldehydes in a one-to-two fashion to give 1,3-diene derivatives.The dienes are produced through (i) addition of the alkyne complexes with 2 equiv of aldehydes at cis vicinal positions of the alkenes and (ii) deoxygenative elimination of 2,7-dioxanioba-4-cycloheptene complexes.