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Two possible lab syntheses of 1-octen-3-ol are: [12] by the Grignard reaction of acrolein and amyl iodide; by the selective reduction of 1-octen-3-one; Biochemically, 1-octen-3-ol is generated from the peroxidation of linoleic acid, catalyzed by a lipoxygenase, followed by cleavage of the resulting hydroperoxide with the help of a hydroperoxide lyase.
Three of these alcohols, 2-methyl-1-butanol, 2-pentanol, and 3-methyl-2-butanol (methyl isopropyl carbinol), contain stereocenters, and are therefore chiral and optically active. The most important amyl alcohol is isoamyl alcohol , the chief one generated by fermentation in the production of alcoholic beverages and a constituent of fusel oil .
Amyl vinyl carbinyl acetate 3-Acetoxy-1-octene 1-Pentylallyl acetate. Identifiers CAS Number. 2442-10-6 ...
tert-amyl alcohol: 2-methylbutan-2-ol; 2-methyl-2-butanol ... In archaic nomenclature, alcohols can be named as derivatives of methanol using "-carbinol" as the ending.
Oct-1-en-3-one (CH 2 =CHC(=O)(CH 2) 4 CH 3), also known as 1-octen-3-one or amyl vinyl ketone, is the odorant that is responsible for the typical "metallic" smell of metals and blood coming into contact with skin. [2]
The nomenclature has now reversed, with "amyl" being more often used to refer to the terminally branched group also called isopentyl, as in amobarbital. A cyclopentyl group is a ring with the formula -C 5 H 9. The name is also used for the pentyl radical, a pentyl group as an isolated molecule. This free radical is only observed in extreme ...
3-Pentanol, diethyl carbinol. ... 3-Pentanol is one of the eight isomers of amyl alcohol. It is found naturally and has a role as a pheromone. [2] See also
cyclobutyl ethynyl methyl carbinol: 515-81-1 C 8 H 12 O: vinyl cyclohexene monoxide: 106-86-5 C 8 H 12 OS: furfuryl isopropyl sulfide: 1883-78-9 C 8 H 12 O 2: allyl tiglate: 7493-71-2 C 8 H 12 O 2: dimedone: 126-81-8 C 8 H 12 O 2: octynoic acid: 5663-96-7 C 8 H 12 O 4: ethyl diacetylacetate: 603-69-0 C 8 H 12 O 8 W 2: ditungsten tetraacetate ...