Trifluoracetonitrile
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Trifluoracetonitrile
Trifluoroacetonitrile is a nitrile with the chemical formula CF3CN. Production Trifluoroacetonitrile can be produced by dehydration of trifluoroacetamide with trifluoroacetic anhydride in pyridine or carbon tetrachloride. This synthesis route was first described by Frédéric Swarts in 1922. Trifluoroacetonitrile can also be produced by reacting 1,1,1-trichloro-2,2,2-trifluoroethane and ammonia Ammonia is an inorganic compound of nitrogen and hydrogen with the formula . A stable binary hydride, and the simplest pnictogen hydride, ammonia is a colourless gas with a distinct pungent smell. Biologically, it is a common nitrogenous wa ... at 610 °C. Properties Trifluoroacetonitrile is a colourless gas that is insoluble in water. Solid trifluoroacetonitrile's crystal structure is orthorhombic. Uses Trifluoroacetonitrile can be used to prepare other chemicals such as 3-(trifluoromethyl)isoquinoline and 2,4-bis(trifluoromethyl)pyrimidine.{{citation, surname1=Kl ...
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Acetonitrile
Acetonitrile, often abbreviated MeCN (methyl cyanide), is the chemical compound with the formula and structure . This colourless liquid is the simplest organic nitrile (hydrogen cyanide is a simpler nitrile, but the cyanide anion is not classed as organic). It is produced mainly as a byproduct of acrylonitrile manufacture. It is used as a polar aprotic solvent in organic synthesis and in the purification of butadiene. The skeleton is linear with a short distance of 1.16  Å. Acetonitrile was first prepared in 1847 by the French chemist Jean-Baptiste Dumas. Applications Acetonitrile is used mainly as a solvent in the purification of butadiene in refineries. Specifically, acetonitrile is fed into the top of a distillation column filled with hydrocarbons including butadiene, and as the acetonitrile falls down through the column, it absorbs the butadiene which is then sent from the bottom of the tower to a second separating tower. Heat is then employed in the separatin ...
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Bulletin Des Sociétés Chimiques Belges
The ''Bulletin des Sociétés Chimiques Belges'' (, CODEN BSCBAG) is the Belgium peer-reviewed scientific journal in chemistry. Originally it started under the name * ''Bulletin de l'Association Belge des Chimistes'' ol. 1 (1887/88) to Vol. 17 (1903) but with Vol. 18 (1904) the title name changed. The journal is also known under the title * ''Bulletin de la Société Chimiques de Belgique''. In 1998 this journal was absorbed by the ''European Journal of Organic Chemistry'' and the ''European Journal of Inorganic Chemistry''. See also * Anales de Química * Chemische Berichte * Bulletin de la Société Chimique de France * European Journal of Organic Chemistry * European Journal of Inorganic Chemistry * Gazzetta Chimica Italiana * Liebigs Annalen * Recueil des Travaux Chimiques des Pays-Bas The ''Recueil des Travaux Chimiques des Pays-Bas'' was the Dutch scientific journal for chemistry. It was established in 1882, but from 1897 (vol. 16) to 1919 (vol 38) it was publis ...
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Trifluoromethyl Compounds
The trifluoromethyl group is a functional group that has the formula -CF3. The naming of is group is derived from the methyl group (which has the formula -CH3), by replacing each hydrogen atom by a fluorine atom. Some common examples are trifluoromethane H–, 1,1,1-trifluoroethane –, and hexafluoroacetone –CO–. Compounds with this group are a subclass of the organofluorines. Properties The trifluoromethyl group has a significant electronegativity that is often described as being intermediate between the electronegativities of fluorine and chlorine. For this reason, trifluoromethyl-substituted compounds are often strong acids, such as trifluoromethanesulfonic acid and trifluoroacetic acid. Conversely, the trifluoromethyl group lowers the basicity of compounds like trifluoroethanol. Uses The trifluoromethyl group occurs in certain pharmaceuticals, drugs, and abiotically synthesized natural fluorocarbon based compounds. The medicinal use of the trifloromethyl group dates from ...
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Liebigs Annalen Der Chemie
''Justus Liebigs Annalen der Chemie'' (often cited as just ''Liebigs Annalen'') was one of the oldest and historically most important journals in the field of organic chemistry worldwide. It was established in 1832 and edited by Justus von Liebig with Friedrich Wöhler and others until Liebig's death in 1873. In 1997 the journal merged with ''Recueil des Travaux Chimiques des Pays-Bas'' to form ''Liebigs Annalen/Recueil''. In 1998 it was absorbed by ''European Journal of Organic Chemistry'' by merger of a number of other national European chemistry journals. Title history * ''Annalen der Pharmacie'', 1832–1839 * ''Annalen der Chemie und Pharmacie'', 1840–1873 (, CODEN JLACBF) * ''Justus Liebig's Annalen der Chemie und Pharmacie'', 1873–1874 (, CODEN JLACBF) * ''Justus Liebig's Annalen der Chemie'', 1874–1944 & 1947–1978 (, CODEN JLACBF) * ''Liebigs Annalen der Chemie'', 1979–1994 (, CODEN LACHDL) * ''Liebigs Annalen'', 1995–1996 (, CODEN LANAEM) * ''Liebi ...
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Journal Of Molecular Spectroscopy
''Journal of Molecular Spectroscopy'' is a peer-reviewed scientific journal that deals with experimental and theoretical articles on all subjects relevant to molecular spectroscopy and its modern applications. Indexing and abstracting According to the ''Journal Citation Reports'', the journal has a 2020 impact factor of 1.507. The journal in indexing in the following bibliographic databases: * AGRICOLA * Chemical Abstracts * Current Contents/Physics, Chemical, & Earth Sciences * Research Alert * Science Abstracts * Science Citation Index * Biological Abstracts * Scopus Scopus is Elsevier's abstract and citation database launched in 2004. Scopus covers nearly 36,377 titles (22,794 active titles and 13,583 inactive titles) from approximately 11,678 publishers, of which 34,346 are peer-reviewed journals in top-l ... References External links * {{Official website, https://www.journals.elsevier.com/journal-of-molecular-spectroscopy/ Optics journals ...
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Orthorhombic Crystal Structure
In crystallography, the orthorhombic crystal system is one of the 7 crystal systems. Orthorhombic lattices result from stretching a cubic lattice along two of its orthogonal pairs by two different factors, resulting in a rectangular prism with a rectangular base (''a'' by ''b'') and height (''c''), such that ''a'', ''b'', and ''c'' are distinct. All three bases intersect at 90° angles, so the three lattice vectors remain mutually orthogonal. Bravais lattices There are four orthorhombic Bravais lattices: primitive orthorhombic, base-centered orthorhombic, body-centered orthorhombic, and face-centered orthorhombic. For the base-centered orthorhombic lattice, the primitive cell has the shape of a right rhombic prism;See , row oC, column Primitive, where the cell parameters are given as a1 = a2, α = β = 90° it can be constructed because the two-dimensional centered rectangular base layer can also be described with primitive rhombic axes. Note that the length a of the primitiv ...
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Ammonia
Ammonia is an inorganic compound of nitrogen and hydrogen with the formula . A stable binary hydride, and the simplest pnictogen hydride, ammonia is a colourless gas with a distinct pungent smell. Biologically, it is a common nitrogenous waste, particularly among aquatic organisms, and it contributes significantly to the nutritional needs of terrestrial organisms by serving as a precursor to 45% of the world's food and fertilizers. Around 70% of ammonia is used to make fertilisers in various forms and composition, such as urea and Diammonium phosphate. Ammonia in pure form is also applied directly into the soil. Ammonia, either directly or indirectly, is also a building block for the synthesis of many pharmaceutical products and is used in many commercial cleaning products. It is mainly collected by downward displacement of both air and water. Although common in nature—both terrestrially and in the outer planets of the Solar System—and in wide use, ammonia is both caust ...
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1,1,1-trichloro-2,2,2-trifluoroethane
Asymmetrical trichlorotrifluoroethane, also called 1,1,1-Trichloro-2,2,2-trifluoroethane or CFC-113a is a chlorofluorocarbon (CFC). It has the formula . Environmental effects Ozone depletion A team of researchers at the University of East Anglia analysed unpolluted air samples from Tasmania dating from the period 1978 to 2012. They concluded that the CFC's they studied had started entering the atmosphere from anthropogenic sources in the 1960s and that while the abundance of certain CFCs had decreased, owing to the Montreal Protocol, the abundance of CFC-113a in the atmosphere was still growing. Its source remained uncertain, but production of hydrofluorocarbons Hydrofluorocarbons (HFCs) are man-made organic compounds that contain fluorine and hydrogen atoms, and are the most common type of organofluorine compounds. Most are gases at room temperature and pressure. They are frequently used in air conditi ... in East Asia was suspected by some. Between 2012 and 2017, concentr ...
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Frédéric Swarts
Frédéric Swarts (2 September 1866 – 6 September 1940) was a Belgian chemist who prepared the first chlorofluorocarbon, CF2Cl2 (Freon-12) as well as several other related compounds. He was a professor in the civil engineering at the University of Ghent. In addition to his work on organofluorine chemistry, he authored the textbook "Cours de Chimie Organique."Frédéric Swarts "Cours de Chimie Organique" Librairie Scientifique, A. Hermann (Paris), 1908. He was a son of Theodore Swarts (chemist, *1839 Antwerpen; †1911 Kortenberg, Belgium) and a colleague of Leo Baekeland Leo Hendrik Baekeland (November 14, 1863 – February 23, 1944) was a Belgian chemist. He is best known for the inventions of Velox photographic paper in 1893, and Bakelite in 1907. He has been called "The Father of the Plastics Industry" .... References * {{DEFAULTSORT:Swarts, Frederic 20th-century Belgian inventors Belgian chemists 1866 births 1940 deaths Academic staff of Ghent Universit ...
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Trifluoromethylisocyanide
Trifluoromethylisocyanide is the chemical compound with the formula CF3NC. It is an isocyanide and a fluorocarbon. Polymerisation occurs even at temperatures below its boiling point of −80 °C. As a ligand in coordination chemistry, this species behaves similarly to carbon monoxide Carbon monoxide (chemical formula CO) is a colorless, poisonous, odorless, tasteless, flammable gas that is slightly less dense than air. Carbon monoxide consists of one carbon atom and one oxygen atom connected by a triple bond. It is the simple .... The compound trifluoracetonitrile (CF3CN) is an isomer to trifluoromethylisocyanide. The nitrile is more stable, as is the usual case. References {{reflist Isocyanides Trifluoromethyl compounds ...
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Synthetic Communications
''Synthetic Communications'' is a peer-reviewed scientific journal covering the synthesis of organic compounds 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 s .... Biochemistry journals Publications established in 1971 English-language journals Taylor & Francis academic journals {{chem-journal-stub ...
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