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The nitronium ion, [NO2]+, is a cation. It is an onium ion because its nitrogen atom has +1 charge, similar to ammonium ion [NH4]+. It is created by the removal of an electron from the paramagnetic nitrogen dioxide molecule NO2, or the protonation of nitric acid HNO3.
In organic chemistry, acetyl is a functional group with the chemical formula −COCH3 and the structure −C(=O)−CH3. It is sometimes represented by the symbol Ac. In IUPAC nomenclature, acetyl is called ethanoyl.
In organic chemistry, a dicarbonyl is a molecule containing two carbonyl groups. Although this term could refer to any organic compound containing two carbonyl groups, it is used more specifically to describe molecules in which both carbonyls are in close enough proximity that their reactivity is changed, such as 1,2-, 1,3-, and 1,4-dicarbonyls. Their properties often differ from those of monocarbonyls, and so they are usually considered functional groups of their own. These compounds can have symmetrical or unsymmetrical substituents on each carbonyl, and may also be functionally symmetrical or unsymmetrical.
In organic chemistry, a methine group or methine bridge is a trivalent functional group =CH−, derived formally from methane. It consists of a carbon atom bound by two single bonds and one double bond, where one of the single bonds is to a hydrogen. The group is also called methyne or methene, but its IUPAC systematic name is methylylidene or methanylylidene.
Molybdenum hexacarbonyl (also called molybdenum carbonyl) is the chemical compound with the formula Mo(CO)6. This colorless solid, like its chromium, tungsten, and seaborgium analogues, is noteworthy as a volatile, air-stable derivative of a metal in its zero oxidation state.
The tellurite ion is TeO2−
3. A tellurite (compound), for example sodium tellurite, is a compound that contains this ion. They are typically colorless or white salts, which in some ways are comparable to sulfite. A mineral with the formula TeO2 is called tellurite.
Chemical Entities of Biological Interest, also known as ChEBI, is a chemical database and ontology of molecular entities focused on 'small' chemical compounds, that is part of the Open Biomedical Ontologies (OBO) effort at the European Bioinformatics Institute (EBI). The term "molecular entity" refers to any "constitutionally or isotopically distinct atom, molecule, ion, ion pair, radical, radical ion, complex, conformer, etc., identifiable as a separately distinguishable entity". The molecular entities in question are either products of nature or synthetic products which have potential bioactivity. Molecules directly encoded by the genome, such as nucleic acids, proteins and peptides derived from proteins by proteolytic cleavage, are not as a rule included in ChEBI.
Thiirane, more commonly known as ethylene sulfide, is the cyclic chemical compound with the formula C2H4S. It is the smallest sulfur-containing heterocycle and the simplest episulfide. Like many organosulfur compounds, this species has a highly unpleasant odour. Thiirane is also used to describe any derivative of the parent ethylene sulfide.
Methylidyne, or (unsubstituted) carbyne, is an organic compound whose molecule consists of a single hydrogen atom bonded to a carbon atom. It is the parent compound of the carbynes, which can be seen as obtained from it by substitution of other functional groups for the hydrogen.
The dithionate (or metabisulfate) anion, S
2O2−
6, is a sulfur oxoanion derived from dithionic acid, H2S2O6. Its chemical formula is sometimes written in a semistructural format, as [O3SSO3]2−. It is the first member of the polythionates.
In chemistry, the hydron, informally called proton, is the cationic form of atomic hydrogen, represented with the symbol H+
. The general term "hydron", endorsed by the IUPAC, encompasses cations of hydrogen regardless of their isotopic composition: thus it refers collectively to protons (1H+) for the protium isotope, deuterons (2H+ or D+) for the deuterium isotope, and tritons (3H+ or T+) for the tritium isotope.
Aluminium hydroxide oxide or aluminium oxyhydroxide, AlO(OH) is found as one of two well defined crystalline phases, which are also known as the minerals boehmite and diaspore. The minerals are important constituents of the aluminium ore, bauxite.
Hexuronic acid is any uronic acid derived from a hexose. These include fructuronic acids, galacturonic acids, glucuronic acids, guluronic acids, iduronic acids, mannuronic acids, and tagaturonic acids.
Aluminium monochloride, or chloridoaluminium is the metal halide with the formula AlCl. Aluminium monochloride as a molecule is thermodynamically stable at high temperature and low pressure only. This compound is produced as a step in the Alcan process to smelt aluminium from an aluminium-rich alloy. When the alloy is placed in a reactor that is heated to 1,300 °C and mixed with aluminium trichloride, a gas of aluminium monochloride is produced.
Chebi may refer to:
Naphthoylindoles are a class of synthetic cannabinoids.
Triphosphane or triphosphine is an inorganic compound having the chemical formula HP(PH2)2. It can be generated from diphosphine but is highly unstable at room temperature:
Trisulfane is the inorganic compound with the formula H2S3. It is a pale yellow volatile liquid with a camphor-like odor. It decomposes readily to hydrogen sulfide and elemental sulfur. It is produced by distillation of the polysulfane oil obtained by acidification of polysulfide salts.
1-Naphthoic acid is an organic compound of the formula C10H7CO2H. It is one of two isomeric monocarboxylic acids of naphthalene, the other one being 2-naphthoic acid. 1-Naphthoic acid is a frequent substrate for C-H activation reactions. In general the hydroxynaphthoic acids are far more useful than the parent. It can be prepared by carboxylation of the Grignard reagent generated from 1-Bromonaphthalene. The name of carboxylate anion, the conjugate base of the acid, is 1-naphthoate; the name of the related acyl group is 1-naphthoyl.
2-Naphthoic acid is an organic compound of the formula C10H7CO2H. It is one of two isomeric carboxylic acid derivatives of naphthalene, the other one being 1-naphthoic acid. It can be prepared by carboxylation of 1-chloronaphthalene. Its pKa is 4.2. The name of carboxylate anion, the conjugate base of the acid, is 2-naphthoate; the name of the related acyl group is 2-naphthoyl.
References
- ↑ "CHEBI:52676 - 1-naphthoyl group". Chemical Entities of Biological Interest (ChEBI).
- ↑ "CHEBI:52675 - 2-naphthoyl group". Chemical Entities of Biological Interest (ChEBI).
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