Название продукции:1-Boc-4-[5-(aminomethyl)-2-pyrimidyl]piperazine

IUPAC Name:tert-butyl 4-[5-(aminomethyl)pyrimidin-2-yl]piperazine-1-carboxylate

CAS:944899-79-0
Молекулярная формула:C14H23N5O2
Чистота:95%+
Номер в каталоге:CM385231
Молекулярная масса:293.37

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Информация о продукции

Номер CAS:944899-79-0
Молекулярная формула:C14H23N5O2
Точка плавления:-
Smiles-код:CC(C)(C)OC(=O)N1CCN(CC1)C1=NC=C(CN)C=N1
Плотность:
Номер в каталоге:CM385231
Молекулярная масса:293.37
Точка кипения:
Номер Mdl:
Хранение:

Category Infos

Piperazines
Piperazine is an organic compound consisting of a six-membered ring containing two nitrogen atoms in opposite positions in the ring. The chemical formula of piperazine is C4H10N2, and it is an important pharmaceutical intermediate. Pyrimidines and piperazines are known to be the backbone of many bulk compounds and important core structures for approved drugs; studies have shown that combining a pyridine ring with a piperazine moiety within a single structural framework enhances biological activity.
Pyrimidines
Pyrimidine, also known as 1,3-diazobenzene, is a heterocyclic compound with the chemical formula C4H4N2. Pyrimidine is formed by substituting 2 nitrogen atoms for 2 carbons in the meta-position of benzene. It is a diazine and retains its aromaticity. Derivatives of pyrimidine widely exist in organic macromolecular nucleic acids, and many drugs also contain pyrimidine rings. In nucleic acids, three nucleobases are pyrimidine derivatives: cytosine, thymine and uracil. There are a variety of pyrimidine-containing drugs on the market, most of which are kinase inhibitors.

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Product Other Information

Product Overview 1-Boc-4-[5-(aminomethyl)-2-pyrimidyl]piperazine (1-Boc-4-AMPP) is a synthetic compound that has been studied for its potential applications in the field of scientific research. It is a piperazine derivative and is used as a building block in the synthesis of various compounds. 1-Boc-4-AMPP has been explored for its ability to modulate the activity of enzymes, receptors, and other proteins, as well as its potential to act as a drug delivery system.
Synthesis and Application 1-Boc-4-[5-(aminomethyl)-2-pyrimidyl]piperazine is synthesized by a two-step process. The first step involves the reaction of 4-aminopiperazine with 2-chloro-5-methylpyrimidine in the presence of triethylamine. This reaction yields 1-Boc-4-[5-(aminomethyl)-2-pyrimidyl]piperazine. The second step involves the hydrolysis of the Boc-protected piperazine to yield the final product. 1-Boc-4-[5-(aminomethyl)-2-pyrimidyl]piperazine has been studied for its potential applications in scientific research. It has been explored as a modulator of enzyme activity, as a drug delivery system, and as a potential therapeutic agent. It has also been studied for its ability to bind to nucleic acids and proteins, as well as its ability to interact with cell membranes.
Future Directions 1-Boc-4-[5-(aminomethyl)-2-pyrimidyl]piperazine has potential applications in scientific research, and there are several potential future directions for its use. These include the development of new drug delivery systems, the exploration of its potential as a therapeutic agent, and the further investigation of its mechanism of action. Additionally, further research is needed to explore the effects of 1-Boc-4-[5-(aminomethyl)-2-pyrimidyl]piperazine on other proteins, as well as its potential interactions with cell membranes. Finally, further research could explore the potential use of 1-Boc-4-[5-(aminomethyl)-2-pyrimidyl]piperazine as a reagent in the synthesis of other compounds.