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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and developed by Eli Lilly and Company and marketed as an inhaled nasal decongestant from 1948 until it was voluntarily withdrawn from the market in the 1980s.
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.
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 ...
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.
Hexane (/ ˈ h ɛ k s eɪ n /) or n-hexane is an organic compound, a straight-chain alkane with six carbon atoms and the molecular formula C 6 H 14. [7]Hexane is a colorless liquid, odorless when pure, and with a boiling point of approximately 69 °C (156 °F).
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.
Phosgene oxime, or CX, is an organic compound with the formula Cl 2 C=N−O H. It is a potent chemical weapon, specifically a nettle agent. The compound itself is a colorless solid, but impure samples are often yellowish liquids. It has a strong, disagreeable and irritating odor. It is used as a reagent in organic chemistry. [2]
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 ...