Название продукции:1-Boc-octahydropyrrolo[3,4-b]pyridine

IUPAC Name:tert-butyl octahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate

CAS:159877-36-8
Молекулярная формула:C12H22N2O2
Чистота:95%+
Номер в каталоге:CM121829
Молекулярная масса:226.32

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Информация о продукции

Номер CAS:159877-36-8
Молекулярная формула:C12H22N2O2
Точка плавления:-
Smiles-код:O=C(N1CCCC2C1CNC2)OC(C)(C)C
Плотность:
Номер в каталоге:CM121829
Молекулярная масса:226.32
Точка кипения:
Номер Mdl:MFCD06858490
Хранение:

Category Infos

Piperidines
Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
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Pyrrolidines
Pyrrolidine, also known as tetrahydropyrrole, is a saturated five-membered heterocyclic ring, which is miscible with water. Pyrrolidine exists in many alkaloids and drug molecules, such as kappa opioids, antagonists of dopamine D4 receptors, and HIV reverse transcriptase inhibitors.

Column Infos

Alicyclic Heterocycles
When the ends of the chains are joined together into a ring, cyclic compounds result; such substances often are referred to as carbocyclic or alicyclic compounds. Substitution of one or more of the ring carbon atoms in the molecules of a carbocyclic compound with a heteroatom gives a heterocyclic compound.

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Product Other Information

Product Overview 1-Boc-octahydropyrrolo[3,4-b]pyridine, also known as BOPP, is a heterocyclic compound. BOPP is widely used in the synthesis of organic compounds and is known for its biological activity.
Synthesis and Application The synthesis of 1-Boc-octahydropyrrolo[3,4-b]pyridine involves the condensation of 1-bromo-4-methylpyrrole and 1-bromo-3-methylpyrrole in the presence of a base and a catalyst. The reaction is carried out in a two-phase system, with the organic layer containing the reactants and the aqueous layer containing the base and catalyst. The reaction is typically conducted at room temperature, and the product is isolated by extraction and purification. 1-Boc-octahydropyrrolo[3,4-b]pyridine has been extensively studied in scientific research due to its biological activity and potential applications. It has been studied as an inhibitor of the enzyme acetylcholinesterase, which is involved in the breakdown of the neurotransmitter acetylcholine. 1-Boc-octahydropyrrolo[3,4-b]pyridine has also been studied as an inhibitor of the enzyme monoamine oxidase, which is involved in the metabolism of monoamine neurotransmitters such as serotonin and dopamine. 1-Boc-octahydropyrrolo[3,4-b]pyridine has also been studied as an antioxidant and as an inhibitor of the enzyme cyclooxygenase, which is involved in the biosynthesis of prostaglandins.
Future Directions There are a number of possible future directions for research on 1-Boc-octahydropyrrolo[3,4-b]pyridine. One potential direction is to further investigate the mechanism of action of 1-Boc-octahydropyrrolo[3,4-b]pyridine, as well as its potential effects on biochemical and physiological processes. Additionally, further research could be conducted to explore the potential applications of 1-Boc-octahydropyrrolo[3,4-b]pyridine, such as its use as an inhibitor of enzymes involved in the metabolism of neurotransmitters. Another potential direction for research is to investigate the toxicity of 1-Boc-octahydropyrrolo[3,4-b]pyridine, as well as ways to reduce its toxicity. Finally, further research could be conducted to explore the potential use of 1-Boc-octahydropyrrolo[3,4-b]pyridine in the synthesis of other compounds.