n
Obsolete spelling of acetonitrile [(organic chemistry) The simplest organic cyanide or nitrile, CH₃CN, formally derived from acetic acid]
n
(organic chemistry) Any organic compound containing an acyl functional group directly attached to a fluorine atom.
n
(organic chemistry) Any radical cation of the form R₃N-⁺
n
(chemistry) The uncharged form of an aminoxide derived from hydroxylamines by removal of a proton; their structure is best represented as R₂NO^. <=> R₂N^(.+)-O⁻.
n
(inorganic chemistry) The univalent inorganic radical cation NH₃^(+.) derived from ammonia; azaniumyl
n
(inorganic chemistry) The univalent inorganic radical cation NH₃^(+.) derived from ammonia; ammoniumyl
n
(organic chemistry) Any anion, salt or ester derived from benzenedicarboxylic acid
n
(organic chemistry) Sometimes used in place of the phenyl group.
n
(biochemistry) Any compound in which one or more hydroxyl groups of a sugar have been replaced by atoms of bromine
n
(organic chemistry) nitrocellulose.
n
(chemistry) any of a class of unstable compounds of nitrogen and chlorine R₁R₂NCl; also the parent compound NH₂Cl, used to manufacture hydrazine, and as the antiseptic chloramine-T
n
(chemistry, in combination) The univalent radical NC- derived from cyanide
n
(chemistry) The radical -CN.
n
(organic chemistry) Any compound having both a hydroxy and a cyanide functional group, especially one having these groups attached to the same carbon atom
adj
(organic chemistry, only in combination) From which a nitro group has been removed
n
(organic chemistry) A clear colourless flammable liquid with a low boiling point, low viscosity, and excellent dissolving power, the dimethyl acetal of formaldehyde.
n
(organic chemistry, especially in combination) Two nitrosyl radicals in a molecule
adj
(organic chemistry) Describing a cyclic peptide having at least one link between amino acids that is other than eupeptide (isopeptide, disulfide, ester etc.)
n
(organic chemistry) A radical derived from organic derivative of hydroxylamine by the removal or a hydrogen atom from the oxygen.
n
(organic chemistry, especially in combination) The univalent radical CH₃-C(=NH)-NH-
n
(organic chemistry) One of a series of compounds containing iodine, and analogous to the chlorhydrins.
n
(organic chemistry) A quaternary ammonium compound that has one or more methyl groups attached to the nitrogen atom
n
(obsolete, organic chemistry) methylamine
n
(organic chemistry, in combination) Any substituted derivative of a methylidene radical
n
(chemistry) any molecular entity having the characteristics of a nitrene or acting as a source of nitrenes
n
(organic chemistry) Synonym of cyanoformate
n
Any alkane containing a nitro group
n
(chemistry) A derivative compound obtained by reaction with nitrogen.
n
(chemistry) The rapid inversion of the lone pair in a molecule such as a tertiary amine which prevents it from being chiral.
n
(chemistry) Ethyl oxamate, obtained as a white scaly crystalline powder.
n
(organic chemistry) An iododestannylation reaction using radioiodine
n
(organic chemistry) Any N-sulfinyl derivative of an amine
n
(organic chemistry) Any N-sulfonyl derivative of an imine
n
(chemistry) A transparent, crystalline compound, (CH₃)₄N⁺Au⁻, obtained by an ion exchange reaction of caesium auride in liquid ammonia.
n
(organic chemistry) The quaternary ammonium base (CH₃)₄N⁺ OH⁻
n
(organic chemistry, especially in combination) The quaternary ammonium cation (CH₃CH₂CH₂)₄N⁺
n
(organic chemistry) A derivative of cytosine in which a hydroxyl group has been replaced by a thiol group
n
(chemistry) solid cyanuric acid
n
(organic chemistry) Any compound that has three epoxide rings
n
(organic chemistry, especially in combination) The univalent cation obtained by protonation of trimethylamine (CH₃)₃NH⁺
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