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Phellandrene
Phellandrenes are organic compounds with the formula . They have a similar molecular structure and similar chemical properties. α-Phellandrene and β-phellandrene are cyclic monoterpenes and are double-bond isomers. In α-phellandrene, both double bonds are endocyclic, and in β-phellandrene, one of them is exocyclic. Both are insoluble in water, but miscible with organic solvents. Etymology and occurrence α-Phellandrene was named after ''Eucalyptus phellandra'', now called '' Eucalyptus radiata'', from which it can be isolated. It is also a constituent of the essential oil of ''Eucalyptus dives''. β-Phellandrene has been isolated from the oil of water fennel and Canada balsam oil. The main source of β-phellandrene is terpentine. β- pinene is a source of β-phellandrene. Reactions and uses α-Phellandrene undergoes hydrochlorination to give phellandrene hydrochloride (a cyclohexenyl chloride). Base hydrolysis of this hydrochloride gives piperitol. The phella ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Phellandrene Mechanism
Phellandrenes are organic compounds with the formula . They have a similar molecular structure and similar chemical properties. α-Phellandrene and β-phellandrene are cyclic terpene, monoterpenes and are double-bond isomers. In α-phellandrene, both double bonds are endocyclic, and in β-phellandrene, one of them is exocyclic. Both are insoluble in water, but miscibility, miscible with organic solvents. Etymology and occurrence α-Phellandrene was named after ''Eucalyptus phellandra'', now called ''Eucalyptus radiata'', from which it can be isolated. It is also a constituent of the essential oil of ''Eucalyptus dives''. β-Phellandrene has been isolated from the oil of fennel, water fennel and Canada balsam oil. The main source of β-phellandrene is terpentine. β-pinene is a source of β-phellandrene. Reactions and uses α-Phellandrene undergoes hydrochlorination to give phellandrene hydrochloride (a cyclohexenyl chloride). Base hydrolysis of this hydrochloride gives pipe ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Eucalyptus Dives
''Eucalyptus dives'', commonly known as the broad-leaved peppermint or blue peppermint, is a species of tree that is Endemism, endemic to south-eastern Australia. It has rough, finely fibrous bark on the trunk and larger branches, smooth bark above, lance-shaped or curved adult leaves, flower buds in groups of eleven or more, white flowers and cup-shaped, hemispherical or conical fruit. Description ''Eucalyptus dives'' is a tree that grows to a height of and forms a lignotuber. The bark on the trunk and larger branches is rough, finely fibrous and greyish and smooth grey on the thinner branches. Young plants and coppice regrowth have leaves arranged in opposite pairs, egg-shaped to heart-shaped or curved, long and wide and Sessility (botany), sessile. Adult leaves are arranged alternately, lance-shaped to curved, the same slightly glossy or dull green on both sides, long and wide on a petiole long. The flower buds are usually arranged in groups of eleven or more in leaf axil ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Eucalyptus Radiata
''Eucalyptus radiata'', commonly known as the narrow-leaved peppermint or Forth River peppermint, is a species of tree that is endemic to south-eastern Australia. It has rough, fibrous to flaky bark on the trunk and larger branches, smooth grey bark on the thinner branches, lance-shaped to curved or almost linear leaves, flower buds in groups of eleven to twenty or more, white flowers and cup-shaped, hemispherical or shortened spherical fruit. Description ''Eucalyptus radiata'' is a tree that typically grows to a height of and forms a lignotuber. It has rough, finely fibrous or flaky grey bark on the trunk and branches, usually smooth grey bark on branches thinner than . Young plants and coppice regrowth have sessile, narrow lance-shaped to linear leaves that are long, wide, paler on the lower surface and arranged in opposite pairs. Adult leaves are the same shade of green on both sides, lance-shaped to curved or almost linear, long and wide, tapering to a petiole long. T ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
(Cymene)ruthenium Dichloride Dimer
(Cymene)ruthenium dichloride dimer is the organometallic compound with the formula cymene)RuCl This red-coloured, diamagnetic solid is a reagent in organometallic chemistry and homogeneous catalysis. The complex is structurally similar to (benzene)ruthenium dichloride dimer. Preparation and reactions The dimer is prepared by the reaction of the phellandrene with hydrated ruthenium trichloride. At high temperatures, cymene)RuClexchanges with other arenes: : cymene)RuCl+ 2 CMe → CMe)RuCl+ 2 cymene (Cymene)ruthenium dichloride dimer reacts with Lewis bases to give monometallic adducts: : cymene)RuCl+ 2 PPh → 2 (cymene)RuCl(PPh) Such monomers adopt pseudo-octahedral piano-stool structures. Precursor to catalysts Treatment of cymene)RuClwith the chelating ligand Ts DPENH gives (cymene)Ru(TsDPEN-H), a catalyst for asymmetric transfer hydrogenation. cymene)RuClis also used to prepare catalysts (by monomerization with dppf) used in borrowing hydrogen catalysis, a cataly ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
The Merck Index
''The Merck Index'' is an encyclopedia of chemicals, drugs and biologicals with over 10,000 monographs on single substances or groups of related compounds published online by the Royal Society of Chemistry. History The first edition of the Merck's Index was published in 1889 by the German chemical company Emanuel Merck and was primarily used as a sales catalog for Merck's growing list of chemicals it sold. The American subsidiary was established two years later and continued to publish it. During World War I the US government seized Merck's US operations and made it a separate American "Merck" company that continued to publish the Merck Index. In 2012 the Merck Index was licensed to the Royal Society of Chemistry. An online version of The Merck Index, including historic records and new updates not in the print edition, is commonly available through research libraries. It also includes an appendix with monographs on organic named reactions. The 15th edition was published in A ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Conjugated Dienes
Conjugation or conjugate may refer to: Linguistics *Grammatical conjugation, the modification of a verb from its basic form *Emotive conjugation or Russell's conjugation, the use of loaded language Mathematics *Complex conjugation, the change of sign of the imaginary part of a complex number * Conjugate (square roots), the change of sign of a square root in an expression *Conjugate element (field theory), a generalization of the preceding conjugations to roots of a polynomial of any degree *Conjugate transpose, the complex conjugate of the transpose of a matrix * Harmonic conjugate in complex analysis * Conjugate (graph theory), an alternative term for a line graph, i.e. a graph representing the edge adjacencies of another graph *In group theory, various notions are called conjugation: **Inner automorphism, a type of conjugation homomorphism **Conjugacy class In mathematics, especially group theory, two elements a and b of a group are conjugate if there is an element g in t ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Monoterpenes
Monoterpenes are a class of terpenes that consist of two isoprene units and have the molecular formula C10H16. Monoterpenes may be linear (acyclic) or contain rings (monocyclic and bicyclic). Modified terpenes, such as those containing oxygen functionality or missing a methyl group, are called monoterpenoids. Monoterpenes and monoterpenoids are diverse. They have relevance to the pharmaceutical, cosmetic, agricultural, and food industries. Biosynthesis Monoterpenes are derived biosynthetically from units of isopentenyl pyrophosphate, which is formed from acetyl-CoA via the intermediacy of mevalonic acid in the HMG-CoA reductase pathway. An alternative, unrelated biosynthesis pathway of IPP is known in some bacterial groups and the plastids of plants, the so-called MEP-(2-methyl-D-erythritol-4-phosphate) pathway, which is initiated from C5 sugars. In both pathways, IPP is isomerized to DMAPP by the enzyme isopentenyl pyrophosphate isomerase. Geranyl pyrophosphate is the precurs ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Elimination Reaction
An elimination reaction is a type of organic reaction in which two substituents are removed from a molecule in either a one- or two-step mechanism. The one-step mechanism is known as the E2 reaction, and the two-step mechanism is known as the E1 reaction. The numbers refer not to the number of steps in the mechanism, but rather to the kinetics of the reaction: E2 is bimolecular (second-order) while E1 is unimolecular (first-order). In cases where the molecule is able to stabilize an anion but possesses a poor leaving group, a third type of reaction, E1cB-elimination reaction, E1CB, exists. Finally, the pyrolysis of xanthate and acetate esters proceed through an "internal" elimination mechanism, the Ei mechanism, Ei mechanism. E2 mechanism The E2 mechanism, where E2 stands for bimolecular elimination, involves a one-step mechanism in which ''carbon-hydrogen'' and ''carbon-halogen'' bonds break to form a double bond (''C=C molecular geometry, Pi bond''). The specifics of the re ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Allyl
In organic chemistry, an allyl group is a substituent with the structural formula . It consists of a methylene bridge () attached to a vinyl group (). The name is derived from the scientific name for garlic, . In 1844, Theodor Wertheim isolated an allyl derivative from garlic oil and named it "". The term allyl applies to many compounds related to , some of which are of practical or of everyday importance, for example, allyl chloride. Allylation is any chemical reaction that adds an allyl group to a Substrate (chemistry), substrate. Nomenclature A site adjacent to the unsaturated carbon atom is called the allylic position or allylic site. A group attached at this site is sometimes described as allylic. Thus, "has an allylic hydroxyl group". Allylic Carbon–hydrogen bond, C−H bonds are about 15% weaker than the C−H bonds in ordinary Orbital hybridisation, sp3 carbon centers and are thus more reactive. Benzylic and allylic are related in terms of structure, bond strength ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Geranyl Pyrophosphate
Geranyl pyrophosphate (GPP), also known as geranyl diphosphate (GDP), is the pyrophosphate ester of the terpenoid geraniol. Its salts are colorless. It is a precursor to many thousands of natural product, natural products. Occurrence GPP is an intermediate in the Terpenoid, isoprenoid biosynthesis pathway that produces longer prenyl chains such as farnesyl pyrophosphate and geranylgeranyl pyrophosphate as well as many Terpene, terpenes. It can be prepared in the laboratory from geraniol. Microbial toxicity Intracellularly produced GPP has been shown to be toxic to the bacteria ''E. coli'' at moderate doses. Related compounds * Geraniol * Farnesyl pyrophosphate * Geranylgeranyl pyrophosphate See also * Dimethylallyltranstransferase References Further reading *Kulkarni RS, Pandit SS, Chidley HG, Nagel R, Schmidt A, Gershenzon J, Pujari KH, Giri AP and Gupta VS, 2013Characterization of three novel isoprenyl diphosphate synthases from the terpenoid rich mango fruit Plant Phy ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
