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Frontalin
Frontalin is a naturally occurring organic compound. It is a terpenoid and acetal that functions as a pheromone in bark beetles and elephants. Occurrence Frontalin acts as an insect pheromone in bark beetles of the genus ''Dendroctonus'', including ''Dendroctonus frontalis'' (''Southern Pine Beetle'') and ''Dendroctonus brevicomis'' (''Western Pine Beetle''), as well as the ''Mountain Pine Beetle''. The biologically active form is predominantly (-)-frontalin. However, (+)-frontalin also occurs in some cases. In ''Dendroctonus frontalis'', the female mainly produces (-)-frontalin, the male mainly (+)-frontalin. In ''Dendroctonus rufipennis'' the distribution is reversed. In addition to its role in insect pheromones, frontalin also serves as a pheromone in Asian elephants. It is secreted by adult male elephants during musth, with secretion levels increasing with age. It signals mating readiness, particularly attracting females who are also in the receptive phase of their sexual ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Asian Elephants
The Asian elephant (''Elephas maximus''), also known as the Asiatic elephant, is the only living species of the genus ''Elephas'' and is distributed throughout the Indian subcontinent and Southeast Asia, from India in the west, Nepal in the north, Sumatra in the south, and to Borneo in the east. Three subspecies are recognised—'' E. m. maximus'' from Sri Lanka, ''E. m. indicus'' from mainland Asia and '' E. m. sumatranus'' from the island of Sumatra. Formerly, there was also the Syrian elephant or Western Asiatic elephant (''Elephas maximus asurus'') which was the westernmost population of the Asian elephant (''Elephas maximus''). This subspecies became extinct in ancient times. Skeletal remains of ''E. m. asurus'' have been recorded from the Middle East: Iran, Iraq, Syria, and Turkey from periods dating between at least 1800 BC and likely 700 BC. It is one of only three living species of elephants or elephantids anywhere in the world, the others being the African bush ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dendroctonus Frontalis
''Dendroctonus frontalis'', the Southern Pine Beetle (also known as SPB), is a species of bark beetle native to the forests of southern United States, Mexico and Central America. The Southern Pine Beetle reddish brown to black exoskeleton and measures approximately , about the size of a grain of rice. It is short-legged, the front of the males head is notched, the female possesses a wide elevated transverse ridge, and the hind abdomen of both is round. Tree infestations ''Dendroctonus frontalis'' inhabits several '' Pinus'' species. Host trees in the United States include primarily '' P. taeda'', '' P. echinata'', '' P. elliottii'', '' P. virginiana'', '' P. rigida'', '' P. palustris'', '' P. serotina'', '' P. pungens'' and '' P. strobus'', '' P. ponderosa'', '' P. engelmannii'' and '' P. leiophylla''. Host trees in Central America include '' P. caribaea'', '' P. engelmannii'', '' P. leiophylla'', '' P. maximinoi'' and '' P. oocarpa''. In the south-eastern United States it is c ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Mole (unit)
The mole, symbol mol, is the unit of amount of substance in the International System of Units (SI). The quantity amount of substance is a measure of how many elementary entities of a given substance are in an object or sample. The mole is defined as containing exactly elementary entities. Depending on what the substance is, an elementary entity may be an atom, a molecule, an ion, an ion pair, or a subatomic particle such as an electron. For example, 10 moles of water (a chemical compound) and 10 moles of mercury (a chemical element), contain equal amounts of substance and the mercury contains exactly one atom for each molecule of the water, despite the two having different volumes and different masses. The number of elementary entities in one mole is known as the Avogadro number, which is the approximate number of nucleons ( protons or neutrons) in one gram of ordinary matter. The previous definition of a mole was simply the number of elementary entities equal to that of 1 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Biosynthesis
Biosynthesis is a multi-step, enzyme- catalyzed process where substrates are converted into more complex products in living organisms. In biosynthesis, simple compounds are modified, converted into other compounds, or joined to form macromolecules. This process often consists of metabolic pathways. Some of these biosynthetic pathways are located within a single cellular organelle, while others involve enzymes that are located within multiple cellular organelles. Examples of these biosynthetic pathways include the production of lipid membrane components and nucleotides. Biosynthesis is usually synonymous with anabolism. The prerequisite elements for biosynthesis include: precursor compounds, chemical energy (e.g. ATP), and catalytic enzymes which may require coenzymes (e.g. NADH, NADPH). These elements create monomers, the building blocks for macromolecules. Some important biological macromolecules include: proteins, which are composed of amino acid monomers joined via pe ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cornforth Reagent
The pyridinium dichromate (PDC) or Cornforth reagent is a pyridinium salt of dichromate with the chemical formula 5H5NHsub>2 r2O7 This compound is named after the Australian-British chemist Sir John Warcup Cornforth (b. 1917) who introduced it in 1962. The Cornforth reagent is a strong oxidizing agent which can convert primary and secondary alcohols to aldehydes and ketones respectively. In its chemical structure and functions it is closely related to other compounds made from hexavalent chromium oxide, such as pyridinium chlorochromate and Collins reagent. Because of their toxicity, these reagents are rarely used nowadays. Synthesis and properties The Cornforth reagent is prepared by slow addition of a concentrated aqueous solution of chromium trioxide to pyridine. The reaction may cause explosion, which is avoided by thoroughly dissolving the trioxide in water and cooling the solution by ice. The product is filtered, washed with acetone and dried, yielding an orange powder. Th ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Hydroxy Group
In chemistry, a hydroxy or hydroxyl group is a functional group with the chemical formula and composed of one oxygen atom covalently bonded to one hydrogen atom. In organic chemistry, alcohols and carboxylic acids contain one or more hydroxy groups. Both the negatively charged anion , called hydroxide, and the neutral radical , known as the hydroxyl radical, consist of an unbonded hydroxy group. According to IUPAC definitions, the term ''hydroxyl'' refers to the hydroxyl radical () only, while the functional group is called a ''hydroxy group''. Properties Water, alcohols, carboxylic acids, and many other hydroxy-containing compounds can be readily deprotonated due to a large difference between the electronegativity of oxygen (3.5) and that of hydrogen (2.1). Hydroxy-containing compounds engage in intermolecular hydrogen bonding increasing the electrostatic attraction between molecules and thus to higher boiling and melting points than found for compounds that lack thi ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Methylmagnesium Bromide
Methylmagnesium chloride is an organometallic compound with the general formula CH3MgCl. This highly flammable, colorless, and moisture sensitive material is the simplest Grignard reagent and is commercially available, usually as a solution in tetrahydrofuran. Synthesis and reactions Relative to the more commonly encountered methylmagnesium bromide and methylmagnesium iodide, methylmagnesium chloride offers the advantages of low equivalent weight and low cost. It is prepared by the reaction of methyl chloride and magnesium in ethyl ether. left, Structure of CH3MgCl(thf)2, which is representative of the species in donor solvents. As with most Grignard reagents, methylmagnesium chloride is highly solvated by ether solvents via coordination from two oxygen atoms to give a tetrahedrally bonded magnesium center. Like methyllithium, it is the synthetic equivalent to the methyl carbanion synthon. It reacts with water and other protic reagents to give methane, e.g.,: :CH3MgCl + ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Lithium Perchlorate
Lithium perchlorate is the inorganic compound with the formula LiClO4. This white or colourless crystalline salt is noteworthy for its high solubility in many solvents. It exists both in anhydrous form and as a trihydrate. Applications Inorganic chemistry Lithium perchlorate is used as a source of oxygen in some chemical oxygen generators. It decomposes at about 400 °C, yielding lithium chloride and oxygen: : LiClO4 → LiCl + 2 O2 Over 60% of the mass of the lithium perchlorate is released as oxygen. It has both the highest oxygen to weight and oxygen to volume ratio of all practical perchlorate salts. Organic chemistry LiClO4 is highly soluble in organic solvents, even diethyl ether. Such solutions are employed in Diels–Alder reactions, where it is proposed that the Lewis acidic Li+ binds to Lewis basic sites on the dienophile, thereby accelerating the reaction. Lithium perchlorate is also used as a co-catalyst in the coupling of α,β-unsaturated carbonyls wit ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chiral Auxiliary
In stereochemistry, a chiral auxiliary is a stereogenic group or unit that is temporarily incorporated into an organic compound in order to control the stereochemical outcome of the synthesis. The chirality present in the auxiliary can bias the stereoselectivity of one or more subsequent reactions. The auxiliary can then be typically recovered for future use. Most biological molecules and pharmaceutical targets exist as one of two possible enantiomers; consequently, chemical syntheses of natural products and pharmaceutical agents are frequently designed to obtain the target in enantiomerically pure form. Chiral auxiliaries are one of many strategies available to synthetic chemists to selectively produce the desired stereoisomer of a given compound. Chiral auxiliaries were introduced by Elias James Corey in 1975 with chiral 8-phenylmenthol and by Barry Trost in 1980 with chiral mandelic acid. The menthol compound is difficult to prepare and as an alternative trans-2-phenyl-1 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Pyruvic Acid
Pyruvic acid (CH3COCOOH) is the simplest of the alpha-keto acids, with a carboxylic acid and a ketone functional group. Pyruvate, the conjugate base, CH3COCOO−, is an intermediate in several metabolic pathways throughout the cell. Pyruvic acid can be made from glucose through glycolysis, converted back to carbohydrates (such as glucose) via gluconeogenesis, or to fatty acids through a reaction with acetyl-CoA. It can also be used to construct the amino acid alanine and can be converted into ethanol or lactic acid via fermentation. Pyruvic acid supplies energy to cells through the citric acid cycle (also known as the Krebs cycle) when oxygen is present ( aerobic respiration), and alternatively ferments to produce lactate when oxygen is lacking. Chemistry In 1834, Théophile-Jules Pelouze distilled tartaric acid and isolated glutaric acid and another unknown organic acid. Jöns Jacob Berzelius characterized this other acid the following year and named pyruvic acid bec ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
