92101-56-9

Basic information

• Product Name: 7-hydroxy-7-phenylheptan-1-ol
• Synonyms: 7-hydroxy-7-phenylheptan-1-ol
• CAS NO: 92101-56-9
• Molecular Weight: 208.301
• Mol File: 92101-56-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 7-hydroxy-7-phenylheptan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 7-hydroxy-7-phenylheptan-1-ol(92101-56-9)
• EPA Substance Registry System: 7-hydroxy-7-phenylheptan-1-ol(92101-56-9)

Safety Data

• Hazardous Substances Data: 92101-56-9(Hazardous Substances Data)

Upstream product

• 717-21-5 3-(furan-1-yl)-1-phenyl-prop-2-en-1-one 
• 100-52-7 benzaldehyde 
• 7472-43-7 6-benzoylhexanoic acid 
• 4286-55-9 1-bromo-6-hexanol 

Downstream Products

• 88773-76-6 7-oxo-7-phenyl-heptanal 
• 712-50-5 Cyclohexyl phenyl ketone 
• 945-49-3 cyclohexylphenylmethanol 

Relevant articles and documents

Takai-Utimoto reactions of oxoalkylhalides catalytic in chromium and cobalt

The scope of chromium(II)/cobalt(I)-catalyzed Takai-Utimoto reactions was extended to substrates with unprotected reactive functional groups. In the presence of a higher chlorosilane and manganese the first chromium(II)/cobalt(I)-catalyzed version for the

Chromium-Catalyzed Linear-Selective Alkylation of Aldehydes with Alkenes

We developed a chromium-catalyzed, photochemical, and linear-selective alkylation of aldehydes with alkylzirconium species generated in situ from a wide range of alkenes and Schwartz's reagent. Photochemical homolysis of the C-Zr bond afforded alkyl radicals, which were then trapped by a chromium complex catalyst to generate the alkylchromium(III) species for polar addition to aldehydes. The reaction proceeded with high functional group tolerance at ambient temperature under visible-light irradiation.