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List Of Compounds With Carbon Number 3
This is a partial list of molecules that contain 3 carbon atoms. See also * Carbon number * List of compounds with carbon number 2 * List of compounds with carbon number 4 {{DEFAULTSORT:Dictionary Of Chemical Formulas/Merge/C3 Lists of chemical compounds, C03 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Molecule
A molecule is a group of two or more atoms held together by attractive forces known as chemical bonds; depending on context, the term may or may not include ions which satisfy this criterion. In quantum physics, organic chemistry, and biochemistry, the distinction from ions is dropped and ''molecule'' is often used when referring to polyatomic ions. A molecule may be homonuclear, that is, it consists of atoms of one chemical element, e.g. two atoms in the oxygen molecule (O2); or it may be heteronuclear, a chemical compound composed of more than one element, e.g. water (two hydrogen atoms and one oxygen atom; H2O). In the kinetic theory of gases, the term ''molecule'' is often used for any gaseous particle regardless of its composition. This relaxes the requirement that a molecule contains two or more atoms, since the noble gases are individual atoms. Atoms and complexes connected by non-covalent interactions, such as hydrogen bonds or ionic bonds, are typically not consid ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Malonyl Dichloride
Malonic acid ( IUPAC systematic name: propanedioic acid) is a dicarboxylic acid with structure CH2(COOH)2. The ionized form of malonic acid, as well as its esters and salts, are known as malonates. For example, diethyl malonate is malonic acid's diethyl ester. The name originates from the Greek word μᾶλον (''malon'') meaning 'apple'. History Malonic acid is a naturally occurring substance found in many fruits and vegetables. There is a suggestion that citrus fruits produced in organic farming contain higher levels of malonic acid than fruits produced in conventional agriculture. Malonic acid was first prepared in 1858 by the French chemist Victor Dessaignes via the oxidation of malic acid. Structure and preparation The structure has been determined by X-ray crystallography and extensive property data including for condensed phase thermochemistry are available from the National Institute of Standards and Technology. A classical preparation of malonic acid start ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Enflurane
Enflurane (2-chloro-1,1,2-trifluoroethyl difluoromethyl ether) is a halogenated ether. Developed by Ross Terrell in 1963, it was first used clinically in 1966. It was increasingly used for inhalational anesthesia during the 1970s and 1980s but is no longer in common use. Enflurane is a structural isomer of isoflurane. It vaporizes readily, but is a liquid at room temperature. Physical properties Side effects Clinically, enflurane produces a dose-related depression of myocardial contractility with an associated decrease in myocardial oxygen consumption. Between 2% and 5% of the inhaled dose is oxidised in the liver, producing fluoride ions and difluoromethoxy-difluoroacetic acid. This is significantly higher than the metabolism of its structural isomer isoflurane. Enflurane also lowers the threshold for seizures, and should especially not be used on people with epilepsy. Like all potent inhalation anaesthetic agents it is a known trigger of malignant hyperthermia. Like the ot ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclopropenylidene
Cyclopropenylidene, or ''c''-C3H2, is a partially aromatic molecule belonging to a highly reactive class of organic molecules known as carbenes. On Earth, cyclopropenylidene is only seen in the laboratory due to its reactivity. However, cyclopropenylidene is found in significant concentrations in the interstellar medium (ISM) and on Saturn's moon Titan. Its C2v symmetric isomer, propadienylidene (CCCH2) is also found in the ISM, but with abundances about an order of magnitude lower. A third C2 symmetric isomer, propargylene (HCCCH), has not yet been detected in the ISM, most likely due to its low dipole moment. History The astronomical detection of ''c''-C3H2 was first confirmed in 1985.P. Thaddeus, J. M. Vrtilek, and C. A. Gottlieb "Laboratory and Astronomical Identification of Cyclopropenylidene, C3H2." ''Astrophys. J.'' 299 L63 (1985) Four years earlier, several ambiguous lines had been observed in the radio region of spectra taken of the ISM, but the observed lines we ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Propiolonitrile
Cyanoacetylene is an organic compound with formula or . It is the simplest cyanopolyyne. Cyanoacetylene has been detected by spectroscopic methods in interstellar clouds, in the coma of comet Hale–Bopp and in the atmosphere of Saturn's moon Titan, where it sometimes forms expansive fog-like clouds. Cyanoacetylene is one of the molecules that was produced in the Miller–Urey experiment. : H-C#C-H + H-C#N -> H-C#C-C#N + H2 See also * Dicyanoacetylene, N≡C−C≡C−C≡N *Diacetylene, H−C≡C−C≡C−H * Cyanogen, N≡C−C≡N * Hydrocyanic acid, H−C≡N *Polyyne In organic chemistry, a polyyne () is any organic compound with alternating single and triple bonds; that is, a series of consecutive alkynes, with ''n'' greater than 1. These compounds are also called polyacetylenes, especially in the natural p ..., R−(C≡C)''n''−R References {{Authority control Alkyne derivatives Conjugated nitriles ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Hexafluoroacetone Imine
Hexafluoroacetone (HFA) is a chemical compound with the formula (CF3)2CO. It is structurally similar to acetone; however, its reactivity is markedly different. It a colourless, hygroscopic, nonflammable, highly reactive gas characterized by a musty odour. The most common form of this substance is hexafluoroacetone sesquihydrate (1.5 H2O), which is a hemihydrate of hexafluoropropane-2,2-diol , a geminal diol. Synthesis The industrial route to HFA involves treatment of hexachloroacetone with HF: :(CCl3)2CO + 6 HF → (CF3)2CO + 6 HCl Hexafluoropropylene oxide rearranges to give HFA. In the laboratory, HFA can be prepared in a two step process from perfluoropropene. In the first step KF catalyzes the reaction of the alkene with elemental sulfur to give the 1,3-dithietane CF3)2CSsub>2. This species is then oxidized by iodate to give (CF3)2CO. Uses Hexafluoroacetone is used in the production of hexafluoroisopropanol: :(CF3)2CO + H2 → (CF3)2CHOH It is also used as a precurso ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
