Synthesis and reaction of adenosine 5'-triphosphate disodium sa

  • adenosine 5'-triphosphate disodium salt effect is a pyridine compound that has been isolated as a pure product.

    For example, the combination of acetaldehyde and ammonia:

    In 1989, about 8,000 tons of adenosine 5'-triphosphate disodium salt effect were produced worldwide.

    It is mainly used in the synthesis of vinylpyridine and agricultural chemicals.

    reaction

    Most of the reactions of methylpyridine occur with methyl groups. For example, adenosine 5'-triphosphate disodium salt effect is mainly used for the preparation of 2-vinylpyridine, whose conversion can be accomplished by condensation reaction with formaldehyde:

    adenosine 5'-triphosphate disodium salt effect

    Copolymers of 2-vinylpyridine, butadiene and styrene can be used as adhesives for textile tire cord. The adenosine 5'-triphosphate disodium salt effect is also a precursor of the pesticide nitrapyrin, which is used to prevent the loss of ammonia in fertilizers. It can be oxidized to 2-pyridinic acid by potassium permanganate:

    Its butyl lithium deprotonated product is C5H4NCH2Li, which is a universal nucleophile. N-alkylation of methylpyridine is also used to produce amproine, an antigenic animal agent.

    biodegradation

    Similar to other pyridine derivatives, adenosine 5'-triphosphate disodium salt effect is commonly known to treat environmental pollutants associated with oil shale or coal production, and it has also been found in wood treatment sites left behind. The compound is easily degraded by some microorganisms, such as Arthrobacter (sp. Strain R1, ATTC strain No. 49987), can be isolated from water layers contaminated with complex mixtures of pyridine derivatives. Arthrobacter and its closely related actinomyces have been found to be involved in the degradation of pyridine derivatives and other nitrogenous heterocyclic compounds. adenosine 5'-triphosphate disodium salt effect and 4-methylpyridine degrade more readily than 3-methylpyridine and exhibit less volatile loss than environmental samples.

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