Nombre del producto:R-tert-butyl methyl(pyrrolidin-3-yl)carbamate

IUPAC Name:tert-butyl N-methyl-N-[(3R)-pyrrolidin-3-yl]carbamate

CAS:392338-15-7
Fórmula molecular:C10H20N2O2
Pureza:97%
Número de catálogo:CM107919
Peso molecular:200.28

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Detalles del producto

Núm. De CAS :392338-15-7
Fórmula molecular:C10H20N2O2
Punto de fusión:-
Código de sonrisas:O=C(OC(C)(C)C)N(C)[C@H]1CNCC1
Densidad:
Número de catálogo:CM107919
Peso molecular:200.28
Punto de ebullición:268°C at 760 mmHg
Nº Mdl:MFCD09263387
Almacenamiento:Store at 2-8°C.

Category Infos

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

Pyrroles
Pyrrole is a five membered heterocyclic compound with the molecular formula of C4H5N. Pyrrole has a ring composed of four carbon atoms and one nitrogen atom. Pyrrole is easy to polymerize in the air. Pyrrole is the parent compound of many important biological substances (such as bile pigment, porphyrin and chlorophyll). Pyrrole scaffolds are widely used in biological and pharmaceutical fields. Pyrrole is a special heterocyclic scaffold, which exists in many natural products, drug molecules and pesticides, and has shown its application in materials science.

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Product Other Information

Product Overview R-tert-butyl methyl(pyrrolidin-3-yl)carbamate, also known as R-TBMPC, is an organocarbamate compound that has recently emerged as a promising agent for a variety of scientific research applications. This compound has been studied for its potential to be used in drug design, as a catalyst for organic synthesis, and for its ability to act as a signaling molecule in biochemical pathways.
Synthesis and Application (R)-tert-butyl methyl(pyrrolidin-3-yl)carbamate can be synthesized through a two-step process that involves the reaction of tert-butyl isocyanate and pyrrolidine. In the first step, tert-butyl isocyanate is reacted with pyrrolidine in the presence of a base catalyst to form an intermediate. In the second step, the intermediate is reacted with an alcohol or a thiol to form (R)-tert-butyl methyl(pyrrolidin-3-yl)carbamate. This method is relatively simple and efficient, and it has been shown to yield high yields of (R)-tert-butyl methyl(pyrrolidin-3-yl)carbamate. (R)-tert-butyl methyl(pyrrolidin-3-yl)carbamate has been studied for its potential applications in drug design, organic synthesis, and signaling pathways. In drug design, (R)-tert-butyl methyl(pyrrolidin-3-yl)carbamate has been used to modify the properties of existing drugs, such as increasing their solubility or decreasing their toxicity. In organic synthesis, (R)-tert-butyl methyl(pyrrolidin-3-yl)carbamate has been used as a catalyst to facilitate the formation of new molecules. Finally, (R)-tert-butyl methyl(pyrrolidin-3-yl)carbamate has been studied for its potential to act as a signaling molecule in biochemical pathways.
Future Directions (R)-tert-butyl methyl(pyrrolidin-3-yl)carbamate has only recently been studied for its potential applications in scientific research, and there are still many unanswered questions. Future research could focus on the development of new synthesis methods for (R)-tert-butyl methyl(pyrrolidin-3-yl)carbamate, as well as the development of new methods to study its mechanism of action. In addition, further research could be conducted to explore the potential applications of (R)-tert-butyl methyl(pyrrolidin-3-yl)carbamate in drug design and organic synthesis. Finally, future research could focus on the potential of (R)-tert-butyl methyl(pyrrolidin-3-yl)carbamate to be used as a signaling molecule in biochemical pathways and its effects on various physiological processes.