Search results
Results from the WOW.Com Content Network
Cyclohexylamine is an organic compound, belonging to the aliphatic amine class. It is a colorless liquid, although, like many amines, samples are often colored due to contaminants.
Hexylamine or n-hexylamine is a chemical compound with the formula CH 3 CH 2 CH 2 CH 2 CH 2 CH 2 NH 2. This colorless liquid is one of the isomeric amines of hexane. At standard temperature and pressure, it has the ammonia/bleach odor common to amines and is soluble in almost all organic solvents.
Methylhexanamine (also known as methylhexamine, 1,3-dimethylamylamine, 1,3-DMAA, dimethylamylamine, and DMAA; trade names Forthane and Geranamine) is an indirect sympathomimetic drug invented and developed by Eli Lilly and Company and marketed as an inhaled nasal decongestant from 1948 until it was voluntarily withdrawn from the market in the 1980s.
Venenivibrio stagnispumantis gains energy by oxidizing hydrogen gas.. In biochemistry, chemosynthesis is the biological conversion of one or more carbon-containing molecules (usually carbon dioxide or methane) and nutrients into organic matter using the oxidation of inorganic compounds (e.g., hydrogen gas, hydrogen sulfide) or ferrous ions as a source of energy, rather than sunlight, as in ...
Chlorination of benzene under electrophilic aromatic substitution conditions (Cl 2 /FeCl 3 or Cl 2 /AlCl 3) produces chlorobenzene.Since mono chloro-de-hydrogenation deactivates the molecule against further electrophilic reactions, the reaction can be halted at one chlorine atom substitution.
The simplest organic chloramine is N-chloromethylamine, CH3NHCl; [7] notable examples include N-chloromorpholine (ClN(CH 2 CH 2) 2 O), N-chloropiperidine, and N-chloroquinuclidinium chloride. [8] Chloramines are commonly produced by the action of sodium hypochlorite on secondary amines: R 2 NH + NaOCl → R 2 NCl + NaOH
3-Chloro-PCP (3'-Cl-PCP) is a recreational designer drug from the arylcyclohexylamine family, with dissociative effects. It has comparable potency to phencyclidine but with a slightly different effects profile, being somewhat more potent as an NMDA antagonist but around the same potency as a dopamine reuptake inhibitor . [ 1 ]
Figure 1. Generally speaking, trimethylenemethane complexes are synthesized in the following four ways: (A) the dehalogenation of α, α'-dihalosubstituted precursors, (B) the thermal extrusion of XY (XY = HCl, Br 2, and CH 4,) from η 3-methylallyl complexes, (C) the ring opening of alkylidenecyclopropanes, and (D) the elimination of Me 3 SiX [X = OAc, Cl, OS(O) 2 Me] from functionalized ...