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  2. IUPAC nomenclature of organic chemistry - Wikipedia

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

    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.

  3. Naringenin - Wikipedia

    en.wikipedia.org/wiki/Naringenin

    Naringenin has the skeleton structure of a flavanone with three hydroxy groups at the 4′, 5, and 7 carbons. [2] It may be found both in the aglycol form, naringenin, or in its glycosidic form, naringin, which has the addition of the disaccharide neohesperidose attached via a glycosidic linkage at carbon 7.

  4. Heterocyclic compound - Wikipedia

    en.wikipedia.org/wiki/Heterocyclic_compound

    A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). [1] Heterocyclic organic chemistry is the branch of organic chemistry dealing with the synthesis, properties, and applications of organic heterocycles .

  5. Sucrose - Wikipedia

    en.wikipedia.org/wiki/Sucrose

    Sucrose is important to the structure of many foods, including biscuits and cookies, cakes and pies, candy, and ice cream and sorbets. It is a common ingredient in many processed and so-called " junk foods ".

  6. Menthone - Wikipedia

    en.wikipedia.org/wiki/Menthone

    The (2S,5S) and (2R,5R) stereoisomers project the isopropyl and methyl groups from the same "side" of the cyclohexane ring, are the so-called cis isomers, and are termed isomenthone; the (2R,5S) and (2S,5R) stereoisomers project the two groups on the opposite side of the ring, are the so-called trans isomers, and are referred to as menthone.

  7. Epoxy - Wikipedia

    en.wikipedia.org/wiki/Epoxy

    The IUPAC name for an epoxide group is an oxirane. Epoxy resins may be reacted ( cross-linked ) either with themselves through catalytic homo polymerisation , or with a wide range of co-reactants including polyfunctional amines, acids (and acid anhydrides ), phenols, alcohols and thiols (sometimes called mercaptans).

  8. Iron sucrose - Wikipedia

    en.wikipedia.org/wiki/Iron_sucrose

    The chemical formula of iron sucrose is C 12 H 29 Fe 5 Na 2 O 23.The iron sucrose molecule is a polymer with two main molecules; sucrose (chemical formula C 12 H 22 O 11) and an iron (III) hydroxide (Na 2 Fe 5 O 8 •3(H 2 O)).

  9. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    Structure All three of these compounds are colorless to white granular solids at room temperature and pressure , but upon exposure to oxygen they may darken. All three isomers have the chemical formula C 6 H 6 O 2 .