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1-Aminopentane is an organic compound with the formula CH 3 (CH 2) 4 NH 2. It is used as a solvent , as a raw material in the manufacture of a variety of other compounds, including dyes, emulsifiers , and pharmaceutical products, [ 1 ] and as a flavoring agent .
It is the N-ethyl analog of 1,3-benzodioxolylpentanamine (BDP; K). Ethyl-K was first synthesized by Alexander Shulgin. In his book PiHKAL ("Phenethylamines i Have Known And Loved"), the minimum dosage is listed as 40 mg and the duration is unknown. [1] [2] Very little is known about the pharmacology, pharmacokinetics, effects, and toxicity of ...
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n-Butylamine is an organic compound (specifically, an amine) with the formula CH 3 (CH 2) 3 NH 2. This colourless liquid is one of the four isomeric amines of butane, the others being sec-butylamine, tert-butylamine, and isobutylamine. It is a liquid having the fishy, ammonia-like odor common to amines.
It can also be prepared by combining ethylene, CO, and H 2. [4] When the reaction is catalyzed by dicobalt octacarbonyl, water can be used as a source of hydrogen.A proposed intermediate is the ethylene-propionyl species [CH 3 C(O)Co(CO) 3 (ethylene)] which undergoes a migratory insertion to form [CH 3 COCH 2 CH 2 Co(CO) 3].
3-Methyl-2-pentanone (methyl sec-butyl ketone) is an aliphatic ketone and isomer of 2-hexanone. [2] References This page was last edited on 17 November 2024, at 23: ...
3-Aminopentane is the organic compound with the formula (CH 3 CH 2) 2 CHNH 2. It is a colorless liquid. It is a colorless liquid. It is of interest for producing soluble imides and imines without introducing a chiral center.
Like other simple aliphatic amines, ethylamine is a weak base: the pK a of [CH 3 CH 2 NH 3] + has been determined to be 10.8 [8] [9] Ethylamine undergoes the reactions anticipated for a primary alkyl amine, such as acylation and protonation. Reaction with sulfuryl chloride followed by oxidation of the sulfonamide give diethyldiazene, EtN=NEt. [10]