enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Chemical graph generator - Wikipedia

    en.wikipedia.org/wiki/Chemical_graph_generator

    These fragments were then used as building blocks in the structure generator. This structure generator was part of a CASE system, ESESOC. [23] Breadth-first search generation. Molecular structure generation is explained step by step. Starting from a set of atoms, bonds are added between atom pairs until reaching saturated structures.

  3. List of chemical databases - Wikipedia

    en.wikipedia.org/wiki/List_of_chemical_databases

    Full name Operator Selects Contains ID prefix Quality Link Entries ACToR Environmental Protection Agency: toxicology information; occurrence "ACToR". 893,280 AtomWork Inorganic Material Database National Institute for Materials Science: crystal structures "AtomWork". 82,000 Beilstein Beilstein database: Elsevier: organic compounds properties ...

  4. 4-Heptanone - Wikipedia

    en.wikipedia.org/wiki/4-Heptanone

    4-Heptanone Names Preferred IUPAC name. Heptan-4-one. Other names Dipropyl ketone, Butyrone, DPK, Propyl ketone ... 4-Heptanone or heptan-4-one is an organic compound ...

  5. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    Because the S 2− anion has a subscript of 2 in the formula (giving a 4− charge), the compound must be balanced with a 4+ charge on the Pb cation (lead can form cations with a 4+ or a 2+ charge). Thus, the compound is made of one Pb 4+ cation to every two S 2− anions, the compound is balanced, and its name is written as lead(IV) sulfide .

  6. Heptanone - Wikipedia

    en.wikipedia.org/wiki/Heptanone

    Heptanone may refer to the following ketones with seven carbon atoms the formula C 7 H 14 O: . 2-Heptanone (Methyl amyl ketone) . 5-Methyl-2-hexanone (Methyl isoamyl ketone); 4-Methyl-2-hexanone (Methyl 2-methylbutyl ketone)

  7. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, the three isomers of xylene CH 3 C 6 H 4 CH 3, commonly the ortho-, meta-, and para-forms, are 1,2-dimethylbenzene, 1,3-dimethylbenzene, and 1,4-dimethylbenzene. The cyclic structures can also be treated as functional groups themselves, in which case they take the prefix "cycloalkyl-" (e.g. "cyclohexyl-") or for benzene, "phenyl-".

  8. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    Alternatively, more explicit structure-based nomenclature can be used when the polymer structure is proven. Where there is no confusion, some traditional names are also acceptable. Whatever method is used, all polymer names have the prefix poly, followed by enclosing marks around the rest of the name. The marks are used in the order: {[( )]}.

  9. 4-Isopropylphenol - Wikipedia

    en.wikipedia.org/wiki/4-Isopropylphenol

    4-Isopropylphenol is an organic compound with the formula (CH 3) 2 CHC 6 H 4 OH. The molecule consists of an isopropyl group affixed to the para ( p -) position of phenol . The compound, a white solid, is produced by the alkylation of phenol with propylene and is relevant to the production of the commodity chemical bisphenol A (BPA).