Evernic Acid
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Evernic Acid
Evernic acid is an organic compound with the molecular formula C17H16O7. Evernic acid was first isolated from the lichen '' Usnea longissima''. Evernic acid is soluble in hot alcohol and bad soluble in water. Evernic acid is produced by the lichens ''Ramalina'', ''Evernia'', and ''Hypogymnia ''Hypogymnia'' is a genus of foliose lichens in the family Parmeliaceae. They are commonly known as tube lichens, bone lichens, or pillow lichens. Most species lack rhizines (root-like attachment organs on the lower surface) that are otherwise c ...''. References Further reading * * * + * * * * * * * * * Polyphenols Methoxy compounds Esters Carboxylic acids {{organic-compound-stub ...
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Organic Compound
In chemistry, organic compounds are generally any chemical compounds that contain carbon- hydrogen or carbon-carbon bonds. Due to carbon's ability to catenate (form chains with other carbon atoms), millions of organic compounds are known. The study of the properties, reactions, and syntheses of organic compounds comprise the discipline known as organic chemistry. For historical reasons, a few classes of carbon-containing compounds (e.g., carbonate salts and cyanide salts), along with a few other exceptions (e.g., carbon dioxide, hydrogen cyanide), are not classified as organic compounds and are considered inorganic. Other than those just named, little consensus exists among chemists on precisely which carbon-containing compounds are excluded, making any rigorous definition of an organic compound elusive. Although organic compounds make up only a small percentage of Earth's crust, they are of central importance because all known life is based on organic compounds. Livin ...
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Usnea Longissima
''Dolichousnea longissima'' (syn. ''Usnea longissima''), commonly known by the names old man's beard or Methuselah's beard lichen, is a fruticose lichen in the family Parmeliaceae. Description This lichen is fruticose, with very long stems and short, even side branches. It is considered the longest lichen in the world. The stems are usually 15 to 30 cm in length but are sometimes much longer. It is pale green to silvery-yellow. It has a distinct central cord, which is white. ''D. longissima'' may grow to be 20 feet in length. It predominantly reproduces asexually through fragmentation. Spore-producing structures are rarely observed. It can double its length each year. Distribution ''Dolichousnea longissima'' is found in boreal forests and coastal woodland in Europe, Asia, and North America. In North America, it is primarily found on the Pacific Coast, and the largest populations are concentrated in the Pacific Northwest. It ranges from Upper Midwest into Canada, the Gre ...
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Ramalina
''Ramalina'' is a genus of greenish fruticose lichens that grow in the form of flattened, strap-like branches. Members of the genus are commonly called strap lichensField Guide to California Lichens, Stephen Sharnoff, Yale University Press, 2014, or cartilage lichens. Apothecia are lecanorine. Lichen spot tests on the cortex are K−, C−, KC+ dark yellow, and P−. It is in the Ramalinaceae and in the suborder Lecanorineae. Distribution The genus has a widespread distribution. A 2008 estimate placed more than 240 species in ''Ramalina''. Species *'' R. ailaoshanensis'' – China *'' R. alisiosae'' – Canary Islands *'' R. americana'' – North America *'' R. andina'' – Venezuela *'' R. arabum'' *'' R. arsenii'' – Europe *'' R. azorica'' – Azores *'' R. australiensis'' *'' R. banzarensis'' *'' R. breviuscula'' *'' R. caespitella'' – Australia *'' R. calcarata'' – East Africa *'' R. calicaris'' *'' R. canalicularis'' *'' R. canariensis'' *'' R. ...
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Evernia
''Evernia'' is a genus of bushy lichens in the family Parmeliaceae. Description Oakmoss ''Evernia prunastri'' is used as a fixative agent in Eau de Cologne within the perfume industry. It is green on top and white on bottom, and divides evenly into "forks"; it becomes very soft when wet. It is not to be confused with ''Ramalina'', which is straplike, stiff and bristly, green on top and bottom, and divides unevenly. ''Evernia'' is an abundant genus, found growing on trees."Evernia." Oregon State University. Retrieved on 25 Sept 2007. References Parmeliaceae Lecanorales genera Lichen genera Taxa named by Erik Acharius Taxa described in 1809 {{Parmeliaceae-stub ...
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Hypogymnia
''Hypogymnia'' is a genus of foliose lichens in the family Parmeliaceae. They are commonly known as tube lichens, bone lichens, or pillow lichens. Most species lack rhizines (root-like attachment organs on the lower surface) that are otherwise common in members of the Parmeliaceae, and have swollen lobes that are usually hollow. Other common characteristics are relatively small spores and the presence of physodic acid and related lichen products. The lichens usually grow on the bark and wood of coniferous trees. ''Hypogymnia'' was proposed by lichenologist William Nylander, first as a subgenus of ''Parmelia'' in 1881, and 15 years later as a distinct genus of two species, including the widespread and common type species, '' Hypogymnia physodes''. It has since grown to about 90 recognized species. ''Hypogymnia'' has a centre of biodiversity in China, where many of its species are found. Taxonomy ''Hypogymnia'' was first created as subgenus of ''Parmelia'' by Finnish lichenologis ...
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Polyphenols
Polyphenols () are a large family of naturally occurring organic compounds characterized by multiples of phenol units. They are abundant in plants and structurally diverse. Polyphenols include flavonoids, tannic acid, and ellagitannin, some of which have been used historically as dyes and for tanning garments. Etymology The name derives from the Ancient Greek word (''polus'', meaning "many, much") and the word phenol which refers to a chemical structure formed by attaching to an aromatic benzenoid (phenyl) ring to a hydroxyl (-OH) group as is found in alcohols (hence the ''-ol'' suffix). The term polyphenol has been in use at least since 1894. Definition The term polyphenol is not well-defined, but is generally agreed that they are natural products "having a polyphenol structure (i.e., several hydroxyl groups on aromatic rings)" including four principal classes: "phenolic acids, flavonoids, stilbenes, and lignans". *Flavonoids include flavones, flavonols, flavanols ...
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Methoxy Compounds
In organic chemistry, a methoxy group is the functional group consisting of a methyl group bound to oxygen. This alkoxy group has the formula . On a benzene ring, the Hammett equation classifies a methoxy substituent at the ''para'' position as an electron-donating group, but as an electron-withdrawing group if at the ''meta'' position. At the ''ortho'' position, steric effects are likely to cause a significant alteration in the Hammett equation prediction which otherwise follows the same trend as that of the ''para'' position. Occurrence The simplest of methoxy compounds are methanol and dimethyl ether. Other methoxy ethers include anisole and vanillin. Many alkoxides contain methoxy groups, e.g. tetramethyl orthosilicate and titanium methoxide. Such compounds are often classified as methoxides. Esters with a methoxy group can be referred to as methyl esters, and the —COOCH3 substituent is called a methoxycarbonyl. Biosynthesis In nature, methoxy groups are found on nucleo ...
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Esters
In chemistry, an ester is a compound derived from an oxoacid (organic or inorganic) in which at least one hydroxyl group () is replaced by an alkoxy group (), as in the substitution reaction of a carboxylic acid and an alcohol. Glycerides are fatty acid esters of glycerol; they are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. They perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Phosphoesters form the backbone of DNA molecules. Nitrate esters, such as nitroglycerin, are known for their explosive properties. '' Nomenclature Etymology Th ...
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