List of chemical compounds with unusual names
From Wikipedia, the free encyclopedia
Chemical nomenclature, replete as it is with compounds with complex names, is a repository for some very peculiar and sometimes startling names. A browse through the Physical Constants of Organic Compounds in the CRC Handbook of Chemistry and Physics (a fundamental resource) will reveal not just the whimsical work of organic chemists, but the sometimes peculiar compound names that occur as the consequence of simple juxtaposition. Some compounds whose names derive legitimately from their chemical makeup or from the geographic region where they may be found include:
- Adamantane (C10H16) a cycloalkane with no connection with Adam Ant;
- Arsole (C4H5As), an analogue of azole in which an arsenic atom replaces the nitrogen atom. Such a replacement in a benzene ring, where the arsenic atom replaces a carbon atom, is known as benzarsole;
- Barrelene (C8H8), the name derives from the obvious resemblance with a barrel;
- Bastardane, a close relative to adamantane and its proper name is ethano-bridged noradamante. Because its unusual ethano-bridge was a variation from the standard hydrocarbon caged rearrangements, it came to be known as bastardane—the unwanted child;
- Buckminsterfullerene or buckyballs, a form of carbon named after Buckminster Fuller due to its resemblance to Fuller's geodesic domes;
- Cadaverine, a foul-smelling diamine produced by putrefaction of dead animal tissue;
- Crapinon, an anticholinergic drug, one side effect of which is constipation;
- Cubane, a hydrocarbon whose eight carbon atoms occupy the vertices of a cube;
- Cummingtonite ((Mg,Fe)7Si8(OH)22), a magnesium-iron silicate hydroxide, first identified in Cummington, Massachusetts;
- DEAD, an apt acronym, given that diethyl azodicarboxylate is explosive; shock sensitive; carcinogenic; and an eye, skin, and respiratory irritant;
- Dickite (Al2Si2O5(OH)4), a clay-like material with a number of manufacturing uses, one of which is as a coating for high-quality bond paper. It is named after its discoverer, Dr. W. Thomas Dick;
- Draculin, an anticoagulant found in the saliva of vampire bats;
- Earthcide or Fartox, two of the many names for pentachloronitrobenzene, a fungicide;
- Fucitol (C6H14O5), an alcohol derived from Fucus vesiculosis, a North Atlantic seaweed. Its optical isomers are also called D-fuc-ol and L-fuc-ol;
- Fukalite (Ca4Si2O6(CO3)(OH,F))2, a rare form of calcium silicocarbonate mined in the Fuka region of Japan;
- Gossypol, a toxin found in cottonseed used as a male contraceptive;
- Megaphone, a ketone derived from the root of Aniba megaphylla;
- Naftazone (C11H9N3O2), a vasoprotective drug. The NAFTA free-trade zone is the area covered by NAFTA;
- Orotic acid (pyrimidinecarboxylic acid), has been referred to as vitamin B13;
- Penguinone, a cyclohexadienone;
- Hirsutene [1] [2] is also named after an animal: a goat (Hircus), occasionally the molecule is depicted upside down [3] [4].
- Performic acid, a strongly oxidizing acid related to formic acid;
- Periodic acid (HIO4), pronounced per-iodic and not periodic (like periodic table). Per denotes that iodine is in the highest possible oxidation state.
- Putrescine, a foul-smelling diamine produced by the putrefaction of dead animal tissue;
- R-CMP, a component of RNA, but also the acronym for the Royal Canadian Mounted Police;
- Skatole, a substance of disagreeable odor that occurs in feces, but also in lower concentrations in flowers, orange blossoms, jasmine;
- Spermine, Spermidine, polyamine growth factors involved in cellular metabolism;
- Titanic acid, the hydrated form of titanium dioxide;
- Traumatic acid, a substance occurring in plants, with a role in healing damaged tissue;
- Unununium (Uuu), the former temporary name of the chemical element number 111, a synthetic transuranium element. This element was named roentgenium (Rg) in November 2004;
[edit] External links
- A more extensive list held at Bristol University;
- Arsole Aromaticity Revisited;
- "Pentachloronitrobenzene", NIST Chemistry Webbook.
[edit] References
- ^ Tandem radical approach to linear condensed cyclopentanoids. Total synthesis of (.+-.)-hirsutene Dennis P. Curran and Donna M. Rakiewicz J. Am. Chem. Soc.; 1985; 107(5) pp 1448 - 1449; DOI:10.1021/ja00291a077
- ^ Isolation, structure and synthesis of hirsutene, a precursor hydrocarbon of coriolin biosynthesis Shigeo Nozoe, Jun Furukawa, Ushio Sankawa and Shoji Shibata Tetrahedron Letters Volume 17, Issue 3 , January 1976, Pages 195-198 DOI:10.1016/0040-4039(76)80013-5
- ^ Hirsutene upside down
- ^ Hirsutene upside down