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ChemAxon Name <> Structure – ChemAxon IUPAC (& traditional) name to structure and structure to IUPAC name software. As used at chemicalize.org; chemicalize.org A free web site/service that extracts IUPAC names from web pages and annotates a 'chemicalized' version with structure images. Structures from annotated pages can also be searched.
benzenesulfonyl chloride: 98-09-9 C 6 H 5 ClSe: phenylselenenyl chloride: 5707-04-0 C 6 H 5 Cl 2 OP: phenylphosphoro dichloridite: 3426-89-9 C 6 H 5 Cl 3 Ge: phenyltrichlorogermane: 1074-29-9 C 6 H 5 Cl 3 Si: phenyl trichlorosilane: 98-13-5 C 6 H 5 Cl 3 Sn: phenyltrichlorostannane: 1124-19-2 C 6 H 5 FO 2 S: benzenesulfonyl fluoride: 368-43-4 C ...
IUPAC nomenclature is used for the naming of chemical compounds, based on their chemical composition and their structure. [1] For example, one can deduce that 1-chloropropane has a Chlorine atom on the first carbon in the 3-carbon propane chain.
Pages in category "Neopentyl compounds" The following 5 pages are in this category, out of 5 total. This list may not reflect recent changes. L. Losmapimod; N.
aluminium chloride fluoride: 22395-91-1 AlCl 2<F: aluminium chloride fluoride: 22395-91-1 AlClO: aluminium chloride oxide: 13596-11-7 AlCl 2 H: dichloroalumane: 16603-84-2 AlCl 3: aluminium chloride: 16603-84-2 AlCl 2 F: aluminium chloride fluoride: 13497-96-6 AlCl 3: aluminium trichloride: 7446-70-0 AlCl 4 Cs: aluminium caesium tetrachloride ...
Neophyl chloride is of interest to organic chemists due to its substitution properties. Neophyl chloride is a neopentyl halide which means it is subject to the neopentyl effect. This effect makes SN 2 nucleophilic substitution highly unlikely because of steric interactions due to the branching of the β-carbon.
For example, for the compound FeCl 3, the cation, iron, can occur as Fe 2+ and Fe 3+. In order for the compound to have a net charge of zero, the cation must be Fe 3+ so that the three Cl − anions can be balanced (3+ and 3− balance to 0). Thus, this compound is termed iron(III) chloride. Another example could be the compound PbS 2.
A full edition was published in 1979, [1] an abridged and updated version of which was published in 1993 as A Guide to IUPAC Nomenclature of Organic Compounds. [2] Both of these are now out-of-print in their paper versions, but are available free of charge in electronic versions.