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Eutylone (also known as β-keto-1,3-benzodioxolyl-N-ethylbutanamine, bk-EBDB, and N-ethylbutylone) is a stimulant and empathogenic drug of the phenethylamine, amphetamine, phenylisobutylamine, and cathinone families which was developed in the 1960s, [3] [4] which is classified as a designer drug. [5]
Butylone can be synthesized in a laboratory via the following route: 3,4-methylenedioxybutyrophenone dissolved in dichloromethane to bromine gives 3′,4′-methylenedioxy-2-bromobutyrophenone. This product was then dissolved in dichloromethane and added to an aqueous solution of methylamine (40%). HCl was then added.
Emoxypine (2-ethyl-6-methyl-3-hydroxypyridine), also known as Mexidol or Mexifin, a succinate salt, is chemical compound which is claimed by its manufacturer, the Russian company Pharmasoft Pharmaceuticals, to have antioxidant and actoprotector properties, [2] [3] but these purported properties of emoxypine have not been proven. [4]
The halogenation of 2-Butyne-1,4-diol [110-65-6] (1) with chlorine gives Mucochloric acid [87-56-9] (2). Treatment with Phenylhydrazine [100-63-0] (3) gives 1-Phenyl-4,5-dichloro-6-pyridazone [1698-53-9] (4). Addition of ammonia leads to Chloridazon [1698-60-8] (5). Catalytic hydrogenation yields 5-amino-2-phenylpyridazin-3-one [13589-77-0] (6).
Butabarbital (brand name Butisol) is a prescription barbiturate sleep aid and anxiety medication.Butabarbital has a particularly fast onset of effects and short duration of action compared to other barbiturates, which makes it useful for certain applications such as treating severe insomnia, relieving general anxiety and relieving anxiety before surgical procedures; however it is also ...
Butyrophenone is an organic compound with the formula C 6 H 5 C(O)C 3 H 7. It is a colorless liquid. It is a colorless liquid. The butyrophenone structure—a ketone flanked by a phenyl ring and a butyl chain —forms the basis for many other chemicals containing various substituents .
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LGD-3303 is a drug which acts as a selective androgen receptor modulator (SARM), with good oral bioavailability. It is a selective agonist for the androgen receptor, producing functional selectivity with effective dissociation of anabolic and androgenic effects, acting as a partial agonist for androgenic effects, but a full agonist for anabolic effects. [1]
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