110631-21-5

Basic information

• Product Name: Benzenemethanol, a-hexyl-2-methyl-
• CAS NO: 110631-21-5
• Molecular Formula: C14H22O
• Molecular Weight: 206.328
• Mol File: 110631-21-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, a-hexyl-2-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-hexyl-2-methyl-(110631-21-5)
• EPA Substance Registry System: Benzenemethanol, a-hexyl-2-methyl-(110631-21-5)

Safety Data

• Hazardous Substances Data: 110631-21-5(Hazardous Substances Data)

Upstream product

• 932-31-0 ortho-tolylmagnesium bromide 
• 111-71-7 heptanal 
• 18379-62-9 dihexylboron chloride 
• 529-20-4 2-methylphenyl aldehyde 

Downstream Products

• 86316-74-7 1-heptyl-2-methyl-benzene 
• 52922-73-3 1-(o-tolyl)-heptan-1-one 
• 120489-00-1 1-hept-1ξ-enyl-2-methyl-benzene 

Relevant articles and documents

Alkylation of aromatic aldehydes with alkylboron chloride derivatives

The reaction of aryl aldehydes with alkylboron chlorides has been investigated. Monoalkylboron dichlorides react with aryl aldehydes in hexane under reflux conditions to give a mixture of dichloroarylmethane and benzyl chloride. Under the same reaction conditions, dialkylboron chlorides lead to formation of a mixture of benzyl chloride and the chloroalkylation product. In the presence of a base such as 2,6-lutidine, the reactions of monoalkylboron dichlorides with aryl aldehydes yield small amounts of the desired alkylation products at room temperature. Dialkylboron chlorides react with aryl aldehydes in hexane in the presence of base to generate the corresponding arylalkylmethanols in good yields.

SUBSTITUTED ETHERS, THIOETHERS AND AMINES FOR USE AS LIPOXYGENASE INHIBITORS

Substituted benzyl ethers, benzyl thioethers, and benzylamines of the formula in which R1 and R2 are identical or different and represent hydrogen, alkyl, alkenyl, cycloalkyl, alkoxy, alkylthio, halogenoalkyl, sulphonylalkyl, halogenoalkoxy, halogenoalkyl