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  2. 1,4-Cyclohexanedicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/1,4-Cyclohexanedi...

    1,4-Cyclohexanedicarboxylic acid describes a pair of organic compounds with the formula C 6 H 10 (CO 2 H) 2. The CO 2 H groups are attached to the opposite carbon centers of the cyclohexane ring. These groups can be cis or trans.

  3. Dicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Dicarboxylic_acid

    Blanc's Rule says that heating a barium salt of a dicarboxylic acid, or dehydrating it with acetic anhydride will yield a cyclic acid anhydride if the carbon atoms bearing acid groups are in position 1 and (4 or 5). So succinic acid will yield succinic anhydride.

  4. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    C 6 H 4 (COOH) 2: benzene-1,4-dicarboxylic acid: terephthalic acid: C 6 H 4 (COOH) 2: 2-methylheptanoic acid C 5 H 11 CH(CH 3)COOH 3-methylheptanoic acid C 4 H 9 CH ...

  5. Cyclohexanecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanecarboxylic_acid

    Cyclohexanecarboxylic acid is a precursor to the nylon-6 precursor caprolactam via its reaction with nitrosylsulfuric acid. It can also be oxidized to cyclohexene. [2] Cyclohexanecarboxylic acid exhibits the reactions typical of carboxylic acids, including its conversion to the acid chloride cyclohexanecarbonyl chloride. [3] [4]

  6. 1,2-Cyclohexane dicarboxylic acid diisononyl ester (DINCH) is a mixture of organic compounds with the formula C 6 H 10 (CO 2 C 9 H 19) 2.DINCH is colorless oil. It is used as a plasticizer for the manufacture of flexible plastic articles in sensitive application areas such as toys, medical devices, and food packaging.

  7. Adipic acid - Wikipedia

    en.wikipedia.org/wiki/Adipic_acid

    Adipic acid or hexanedioic acid is the organic compound with the formula (CH 2) 4 (COOH) 2.From an industrial perspective, it is the most important dicarboxylic acid: about 2.5 billion kilograms of this white crystalline powder are produced annually, mainly as a precursor for the production of nylon.

  8. Decarboxylation - Wikipedia

    en.wikipedia.org/wiki/Decarboxylation

    The Knoevenagel condensation and they allow keto acids serve as a stabilizing protecting group for carboxylic acid enols. [ 6 ] [ page needed ] [ 4 ] For the free acids, conditions that deprotonate the carboxyl group (possibly protonating the electron-withdrawing group to form a zwitterionic tautomer ) accelerate decarboxylation. [ 7 ]

  9. Cyclohexane-1,2,3,4,5,6-hexol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane-1,2,3,4,5,6-hexol

    Cyclohexane-1,2,3,4,5,6-hexol is a family of chemical compounds with formula C 6 H 12 O 6, whose molecule consists of a ring of six carbon atoms, each bound to one hydrogen atom and one hydroxyl group (–OH). There are nine stereoisomers, that differ by the position of the hydroxyl groups relative to the mean plane of the ring.

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