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  2. Transition metal complexes of 1,10-phenanthroline - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_complexes...

    1,10-Phenanthroline is an inhibitor of metallopeptidases, with one of the first observed instances reported in carboxypeptidase A. [11] Inhibition of the enzyme occurs by removal and chelation of the metal ion required for catalytic activity, leaving an inactive apoenzyme . 1,10-Phenanthroline targets mainly zinc metallopeptidases, with a much ...

  3. 1,10-Phenanthroline - Wikipedia

    en.wikipedia.org/wiki/1,10-Phenanthroline

    1,10-Phenanthroline (phen) is a heterocyclic organic compound. It is a white solid that is soluble in organic solvents. It is a white solid that is soluble in organic solvents. The 1,10 refer to the location of the nitrogen atoms that replace CH's in the hydrocarbon called phenanthrene .

  4. Tetramethyl acetyloctahydronaphthalenes - Wikipedia

    en.wikipedia.org/wiki/Tetramethyl...

    Tetramethyl acetyloctahydronaphthalenes (International Nomenclature for Cosmetic Ingredients name) (1-(1,2,3,4,5,6,7,8-ottaidro-2,3,8,8,-tetrametil-2-naftil)etan-1-one) is a synthetic ketone fragrance also known as OTNE (octahydrotetramethyl acetophenone) and by other commercial trade names such as: Iso E Super, Iso Gamma Super, Anthamber, Amber Fleur, Boisvelone, Iso Ambois, Amberlan, Iso ...

  5. Ferroin - Wikipedia

    en.wikipedia.org/wiki/Ferroin

    Ferroin is the chemical compound with the formula [Fe(o-phen) 3]SO 4, where o-phen is an abbreviation for 1,10-phenanthroline, a bidentate ligand. The term "ferroin" is used loosely and includes salts of other anions such as chloride. [1] Ferroin is one of many transition metal complexes of 1,10-phenanthroline.

  6. 1,10-Phenanthroline-5,6-dione - Wikipedia

    en.wikipedia.org/wiki/1,10-Phenanthroline-5,6-dione

    1,10-Phenanthroline-5,6-dione is an organic compound with the formula C 12 H 6 O 2 N 2. It is the quinone derivative of 1,10-phenanthroline . The compound exhibits many reactions, including condensations with diamines to give quinoxalines and decarbonylation to give a diazafluorenone .

  7. 3,3,4,4-Tetramethyltetrahydrofuran-2,5-dione - Wikipedia

    en.wikipedia.org/wiki/3,3,4,4-tetramethyltetra...

    The compound was described in 1890 by Karl von Auwers and Victor Meyer who obtained it by thermal decomposition of 2,2,3,3-tetramethylsuccinic acid. [ 1 ] [ 5 ] It can also be obtained, in > 50% yield, from 3,3,4,4-tetramethylpyrrolidine-2,5-dione [ 4 ] Other synthesis routes include

  8. Triphenylmethanol - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethanol

    Triphenylmethanol features three phenyl (Ph) rings and an alcohol group bound to a central tetrahedral carbon atom. All three C–Ph bonds are typical of sp 3-sp 2 carbon-carbon bonds with lengths of approximately 1.47 Å, while the C–O bond length is approximately 1.42 Å.

  9. 1,3,5,7-Tetramethyl-1,3,5,7-tetrasilaadamantane - Wikipedia

    en.wikipedia.org/wiki/1,3,5,7-tetramethyl-1,3,5...

    1,3,5,7-Tetramethyl-1,3,5,7-tetrasilaadamantane is the organosilicon compound with the formula (CH 2) 6 (SiCH 3) 4. It is a colorless solid that is soluble in organic solvents. The compound is one of the iconic carbosilanes, featuring alternating −Si−C−Si−C− linkages. [2] Otherwise it can be described as a diamondoid cluster.