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  2. Methoxy group - Wikipedia

    en.wikipedia.org/wiki/Methoxy_group

    In nature, methoxy groups are found on nucleosides that have been subjected to 2′-O-methylation, for example in variations of the 5′-cap structure known as cap-1 and cap-2. They are also common substituents in O -methylated flavonoids , whose formation is catalyzed by O-methyltransferases that act on phenols , such as catechol- O -methyl ...

  3. Cyclooctadiene iridium methoxide dimer - Wikipedia

    en.wikipedia.org/wiki/Cyclooctadiene_iridium_m...

    Cyclooctadiene iridium methoxide dimer is an organoiridium compound with the formula Ir 2 (OCH 3) 2 (C 8 H 12) 2, where C 8 H 12 is the diene 1,5-cyclooctadiene. It is a yellow solid that is soluble in organic solvents. The complex is used as a precursor to other iridium complexes, some of which are used in homogeneous catalysis. [1]

  4. List of abbreviations used in medical prescriptions - Wikipedia

    en.wikipedia.org/wiki/List_of_abbreviations_used...

    mistaken for U, meaning units; also has an ambiguous meaning; use "mL" or "millilitres" (1 cm 3 = 1 mL) cf. confer compare c.n. cras nocte: tomorrow night cochl. cochleare: spoonful cochl. ampl. cochleare amplum: an ample spoonful (a tablespoonful) cochl. infant. cochleare infantis: a small spoonful (a teaspoonful) cochl. mag. cochleare magnum

  5. Tetramethyl orthosilicate - Wikipedia

    en.wikipedia.org/wiki/Tetramethyl_orthosilicate

    Tetramethyl orthosilicate (TMOS) is the chemical compound with the formula Si(OCH 3) 4.This molecule consists of four methoxy groups bonded to a silicon atom. The basic properties are similar to the more popular tetraethyl orthosilicate, which is usually preferred because the product of hydrolysis, ethanol, is less toxic than methanol.

  6. Infrared spectroscopy correlation table - Wikipedia

    en.wikipedia.org/wiki/Infrared_spectroscopy...

    1,1-disub. alkenes 1655 medium cis-1,2-disub. alkenes 1660 medium trans-1,2-disub. alkenes 1675 medium trisub., tetrasub. alkenes 1670 weak conjugated C═C dienes 1600 strong 1650 strong with benzene ring 1625 strong with C═O 1600 strong C═C (both sp 2) any 1640–1680 medium aromatic C═C any 1450 weak to strong (usually 3 or 4) 1500 1580

  7. IUPAC nomenclature of organic chemistry - Wikipedia

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

    The secondary functional groups are: a hydroxy- at carbon 5, a chloro- at carbon 11, a methoxy- at carbon 15, and a bromo- at carbon 18. Grouped with the side chains, this gives 18-bromo-12-butyl-11-chloro-4,8-diethyl-5-hydroxy-15-methoxy. There are two double bonds: one between carbons 6 and 7, and one between carbons 13 and 14.

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  9. Orders of magnitude (molar concentration) - Wikipedia

    en.wikipedia.org/wiki/Orders_of_magnitude_(molar...

    neutrinos during a supernova, 1 AU from the core (10 58 over 10 s) [18] 44.6 mM: pure ideal gas at 0 °C and 101.325 kPa [19] 10 −1: dM: 140 mM: sodium ions in blood plasma [10] 480 mM: sodium ions in seawater [20] 10 0: M: 1 M: standard state concentration for defining thermodynamic activity [21] 10 1: daM 17.5 M pure (glacial) acetic acid ...