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2,4-Dibromophenol
2,4-Dibromophenol is a brominated derivative of phenol with the molecular formula C6H4Br2O. It belongs to the bromobenzenes, which are organic compounds containing bromine atoms attached to a benzene ring. Properties At room temperature, 2,4-dibromophenol is a solid with needle-like crystals. It melts at and boils at . it has a molecular weight of 251.905 g/mol. It is soluble in water, ethanol, ether and benzene and slightly soluble in carbon tetrachloride. Occurrence 2,4-Dibromophenol is found in certain molluscs and crustaceans, as well as the acorn worm The acorn worms or Enteropneusta are a Hemichordata, hemichordate class of invertebrates consisting of one order of the same name. The closest non-hemichordate relatives of the Enteropneusta are the echinoderms. There are 111 known species of aco ... '' Saccoglossus bromophenolosus'', which is named after it. References {{DEFAULTSORT:Dibromophenol, 2,4- Phenols Bromoarenes ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Bromine
Bromine is a chemical element with the symbol Br and atomic number 35. It is the third-lightest element in group 17 of the periodic table (halogens) and is a volatile red-brown liquid at room temperature that evaporates readily to form a similarly coloured vapour. Its properties are intermediate between those of chlorine and iodine. Isolated independently by two chemists, Carl Jacob Löwig (in 1825) and Antoine Jérôme Balard (in 1826), its name was derived from the Ancient Greek (bromos) meaning "stench", referring to its sharp and pungent smell. Elemental bromine is very reactive and thus does not occur as a native element in nature but it occurs in colourless soluble crystalline mineral halide salts, analogous to table salt. In fact, bromine and all the halogens are so reactive that they form bonds in pairs—never in single atoms. While it is rather rare in the Earth's crust, the high solubility of the bromide ion (Br) has caused its accumulation in the oceans. Commercial ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Phenol
Phenol (also called carbolic acid) is an aromatic organic compound with the molecular formula . It is a white crystalline solid that is volatile. The molecule consists of a phenyl group () bonded to a hydroxy group (). Mildly acidic, it requires careful handling because it can cause chemical burns. Phenol was first extracted from coal tar, but today is produced on a large scale (about 7 billion kg/year) from petroleum-derived feedstocks. It is an important industrial commodity as a precursor to many materials and useful compounds. It is primarily used to synthesize plastics and related materials. Phenol and its chemical derivatives are essential for production of polycarbonates, epoxies, Bakelite, nylon, detergents, herbicides such as phenoxy herbicides, and numerous pharmaceutical drugs. Properties Phenol is an organic compound appreciably soluble in water, with about 84.2 g dissolving in 1000 mL (0.895 M). Homogeneous mixtures of phenol and water at phenol ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Acorn Worm
The acorn worms or Enteropneusta are a Hemichordata, hemichordate class of invertebrates consisting of one order of the same name. The closest non-hemichordate relatives of the Enteropneusta are the echinoderms. There are 111 known species of acorn worm in the world, the main species for research being ''Saccoglossus kowalevskii''. Two families—Harrimaniidae and Ptychoderidae—separated at least 370 million years ago. Until recently, it was thought that all species Fauna (animals)#Infauna, lived in the sediment on the seabed, subsisting as deposit feeders or suspension feeders. However, the early 21st century has seen the description of a new family, the Torquaratoridae, evidently limited to the deep sea, in which most of the species crawl on the surface of the ocean bottom and alternatively rise into the water column, evidently to drift to new foraging sites. It is assumed that the ancestors of acorn worms used to live in tubes like their relatives Pterobranchia, but that they ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Saccoglossus Bromophenolosus
''Saccoglossus bromophenolosus'' is a species of acorn worm (class Enteropneusta) occurring in the northwestern Atlantic Ocean and the northeastern Pacific Ocean. It grows to a length of about and lives in a burrow in soft sediment in the intertidal and subtidal zones. The scientific name refers to 2,4-dibromophenol, a secondary metabolite present in this worm. Description Like other acorn worms, this soft cylindrical worm is divided into three parts, the proboscis, the collar and the trunk. The proboscis is long and slender with a groove along the top. The mouth is located on the underside where it joins the thick, fleshy collar. A fold at the back of the collar overhangs the trunk, and the anus is at the tip of the trunk. The total length is up to , the proboscis is white to beige, the collar is orange, red or reddish-green and the trunk is either brownish-green or rather pale. Distribution and habitat The species is native to the northwestern Atlantic Ocean where its range ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Phenols
In organic chemistry, phenols, sometimes called phenolics, are a class of chemical compounds consisting of one or more hydroxyl groups (— O H) bonded directly to an aromatic hydrocarbon group. The simplest is phenol, . Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule. Phenols are both synthesized industrially and produced by plants and microorganisms. Properties Acidity Phenols are more acidic than typical alcohols. The acidity of the hydroxyl group in phenols is commonly intermediate between that of aliphatic alcohols and carboxylic acids (their pKa is usually between 10 and 12). Deprotonation of a phenol forms a corresponding negative phenolate ion or phenoxide ion, and the corresponding salts are called phenolates or phenoxides (aryloxides according to the IUPAC Gold Book). Condensation with aldehydes and ketones Phenols are susceptible to Electrophilic aromatic substitutions. Condensation with formald ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
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