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  2. 2,6-Dimethylnaphthalene - Wikipedia

    en.wikipedia.org/wiki/2,6-Dimethylnaphthalene

    2,6-Dimethylnaphthalene is mainly used for the preparation of 2,6-naphthalenedicarboxylic acid by oxidation of 2,6-dimethylnaphthalene in the liquid phase. 2,6-Naphthalenedicarboxylic acid is a monomer for the production of high-performance polymers, in particular poly (ethylene-2,6-naphthalene dicarboxylate) or shorter polyethylene naphthalate (PEN). [4]

  3. 2,6-Naphthalenedicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/2,6-Naphthalenedi...

    It was first prepared by Robert Evert and Victor Merz in 1876 by hydrolysis of 2,6-dicyanonaphthalene. [2] [3] 1,8-Naphthalenedicarboxylic acid can be isomerized to 2,6-naphthalenedicarboxylic acid via the intermediacy of the dipotassium dicarboxylates. [2] It is also produced by oxidation of 2,6-diisopropylnaphthalene. [4]

  4. DMMDA - Wikipedia

    en.wikipedia.org/wiki/DMMDA

    DMMDA-3 could be made from exalatacin (1-allyl-2,6-dimethoxy-3,4-methylenedioxybenzene). Exalatacin can be found in the essential oil of both Crowea exalata and Crowea angustifolia var. angustifolia. [6] In other words, exalatacin is an isomer of both apiole and dillapiole, which can be used to make

  5. 1,6-Bis (2,3-epoxypropoxy)naphthalene - Wikipedia

    en.wikipedia.org/wiki/1,6-bis(2,3-epoxypropoxy...

    1,6-Bis(2,3-epoxypropoxy)naphthalene is a naphthalene-type epoxy resin which is used in many industrial applications. Occupational allergic contact dermatitis has been reported. Occupational allergic contact dermatitis has been reported.

  6. Diaminonaphthalene - Wikipedia

    en.wikipedia.org/wiki/Diaminonaphthalene

    Diaminonaphthalene describes several isomers containing naphthalene substituted with two amine groups (NH 2), also called naphthalenediamines. All isomers are white solids that tend to air-oxidize. The 2,3-, 1,5-, and 1,8- derivatives have attracted most attention. 1,2-Diaminonaphthalene 938-25-0 [1] 1,3-Diaminonaphthalene 24824-28-0 [2]

  7. Dimethoxyethane - Wikipedia

    en.wikipedia.org/wiki/Dimethoxyethane

    Structure of the coordination complex NbCl 3 (dimethoxyethane)(3-hexyne). [5] Together with a high-permittivity solvent (e.g. propylene carbonate), dimethoxyethane is used as the low-viscosity component of the solvent for electrolytes of lithium batteries. In the laboratory, DME is used as a coordinating solvent.

  8. Man allegedly called 911 a total of 17 times and demanded a ...

    www.aol.com/man-allegedly-called-911-total...

    This guy gave new meaning to the slogan “Gottahava Wawa.” Police in East Windsor, N.J., arrested a 24-year-old man on Dec. 23, and charged him with misusing the town’s 911 system for ...

  9. Benzhydryl compounds - Wikipedia

    en.wikipedia.org/wiki/Benzhydryl_compounds

    Ball-and-stick model of diphenylmethane. The benzhydryl compounds are a group of organic compounds whose parent structures include diphenylmethane (which is two benzene rings connected by a single methane), with any number of attached substituents, including bridges.