13732-85-9

Basic information

• Product Name: 2-methyl-6-phenyl-hexan-2-ol
• Synonyms: 2-methyl-6-phenyl-hexan-2-ol
• CAS NO: 13732-85-9
• Molecular Weight: 192.301
• Mol File: 13732-85-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-methyl-6-phenyl-hexan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-6-phenyl-hexan-2-ol(13732-85-9)
• EPA Substance Registry System: 2-methyl-6-phenyl-hexan-2-ol(13732-85-9)

Safety Data

• Hazardous Substances Data: 13732-85-9(Hazardous Substances Data)

Upstream product

• 917-64-6 methyl magnesium iodide 
• 20620-59-1 5-phenyl-n-valeric acid methyl ester 
• 13633-20-0 2-Hydroxy-2-methyl-6-phenyl-hexadien-(3,4) 
• 13633-25-5 1-Bromo-4-phenylbutane 
• 67-64-1 acetone 
• 79889-19-3 2-methyl-6-phenyl-2-hexyl hydroperoxide 
• 690-94-8 dimethyl(vinylethynyl)carbinol 
• 591-51-5 phenyllithium 
• 2270-20-4 5-Phenylpentanoic acid 
• 3360-41-6 4-phenyl-butan-1-ol 
• 103-63-9 1-phenyl-2-bromoethane 
• 75-16-1 methylmagnesium bromide 
• 917-54-4 methyllithium 
• 10521-91-2 5-phenylpentan-1-ol 

Downstream Products

• 36748-60-4 1-Isopropyltetralin 
• 1439367-55-1 1,1-dimethyl-5-phenylpentyl-1-yl pyridin-2-yl carbonate 
• 1439367-56-2 (1,1-dimethyl-5-phenyl-pentyl) 2-oxopyridine-1-carboxylate 
• 1439366-75-2 (1,1-dimethyl-5-phenyl-pentyl) N-[(2S,3R)-2-methyl-4-oxo-oxetan-3-yl]-carbamate 
• 97847-89-7 (1,1-dimethyl-5-phenyl-pentyl)-amine hydrochloride 
• 1430423-76-9 C₁₂H₁₇FO 
• 79889-26-2 3,3-Dimethyl-7-phenyl-[1,2]dioxepane 
• 79889-19-3 2-methyl-6-phenyl-2-hexyl hydroperoxide 

Relevant articles and documents

An Iron-Mesoionic Carbene Complex for Catalytic Intramolecular C-H Amination Utilizing Organic Azides

The synthesis of N-heterocycles is of paramount importance for the pharmaceutical industry. They are often synthesized through atom economic and environmentally unfriendly methods, generating significant waste. A less explored, but greener, alternative is

SUBSTITUTED BENZOXAZOLONE DERIVATIVES AS ACID CERAMIDASE INHIBITORS, AND THEIR USE AS MEDICAMENTS

The present invention relates to substituted benzoxazolone derivatives as acid ceramidase inhibitors, pharmaceutical compositions containing these inhibitors and methods of inhibiting acid ceramidase for the treatment of disorders in which modulation of the levels of ceramide is clinically relevant. The invention also provides substituted benzoxazolone derivatives for use in the treatment of cancer, inflammation, pain, inflammatory pain or pulmonary diseases.

The reaction of alkyl peroxy radicals

Secondary alkyl peroxy radicals generated from 4-phenyl-2-butyl-, 2-nonyl- and 3α-cholestanyl hydroperoxides at 45°C undergo Russell termination reactions in preference to non-terminating decomposition reactions. Non-terminating decomposition of 2-nonyl peroxy radicals afforded 2,5-nonanedione and 2,5-nonanediol due to intramolecular hydrogen abstraction reactions of alkoxy radicals. The radicals derived from 2-methyl-4-phenyl-2-butyl-, 2-methyl-5-phenyl-2-pentyl- and 2-methyl-6-phenyl-2-hexyl hydroperoxides afforded benzylic functionalized products due to intermolecular reactions. 2-Hexylperoxy radicals generated in excess alcohols ineffectively abstracted the α-hydrogens of alcohols. These results demonstrate the low reactivity of alkyl peroxy radicals.