107613-28-5

Basic information

• Product Name: (±)-2-benzyl-1-octanol
• Synonyms: (±)-2-benzyl-1-octanol
• CAS NO: 107613-28-5
• Molecular Weight: 220.355
• Mol File: 107613-28-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (±)-2-benzyl-1-octanol(CAS DataBase Reference)
• NIST Chemistry Reference: (±)-2-benzyl-1-octanol(107613-28-5)
• EPA Substance Registry System: (±)-2-benzyl-1-octanol(107613-28-5)

Safety Data

• Hazardous Substances Data: 107613-28-5(Hazardous Substances Data)

Upstream product

• 111-87-5 octanol 
• 100-51-6 benzyl alcohol 
• 15327-07-8 2-benzyloctanoic acid 
• 15374-23-9 diethyl 2-benzyl-2-hexylmalonate 
• 638-45-9 1-Iodohexane 
• 607-81-8 diethyl 2-benzylmalonate 
• 101-86-0 α-hexylcinnamaldehyde 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 124-13-0 Octanal 

Downstream Products

• 68922-15-6 C₁₂H₂₂O₄ 
• 63450-32-8 (±)-dihydro-4-hexyl-2(3H)-furanone 

Relevant articles and documents

Cross β-alkylation of primary alcohols catalysed by DMF-stabilized iridium nanoparticles

A simple method for the cross β-alkylation of linear alcohols with benzyl alcohols in the presence of DMF-stabilized iridium nanoparticles was developed. The nanoparticles were prepared in one-step and thoroughly characterized. Furthermore, the optimum reaction conditions have a wide substrate scope and excellent product selectivity.

Synthesis and olfactory evaluation of optically active β-alkyl substituted γ-lactones and whiskey lactone analogues

Optically active β-alkyl substituted γ-lactones and whiskey lactone analogues were synthesized, and the odor properties were evaluated. During the preparation of the chiral intermediates, we found good reaction conditions for the highly enantioselective esterification of 3-arylmethyl-2-methyl-1-propanols to kinetically resolve them. The results of the olfactory evaluations of the synthesized lactones revealed that the alkyl groups on the γ-lactone rings played an important role for the odor profiles.

Colloidal palladium nanoparticles with in situ H2: Reducing system for ,-unsaturated carbonyl compounds

A new reducing system comprising Pd(OAc)2 and NaBH4 in methanol to generate palladium nanoparticles has been efficiently utilized to reduce a variety of unsaturated carbonyl compounds. These were reduced to their corresponding saturated alcohols and fully saturated compounds in selected cases. This protocol presents alternative and mild reaction conditions for reduction.