CAS 127294-73-9
:(R)-3-Aminopiperidine
Description:
(R)-3-Aminopiperidine is a chiral amine with a piperidine ring structure, characterized by the presence of an amino group at the 3-position. This compound is notable for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its ability to act as a building block for various bioactive molecules. The (R) configuration indicates that it has a specific spatial arrangement of atoms, which can influence its biological activity and interaction with receptors. It is typically a colorless to pale yellow liquid or solid, depending on its form, and is soluble in polar solvents. The compound exhibits basic properties due to the amino group, allowing it to participate in various chemical reactions, such as alkylation and acylation. Its molecular structure contributes to its role in synthesizing compounds with potential therapeutic effects, making it of interest in drug discovery and development. Safety and handling precautions should be observed, as with many amines, due to potential toxicity and reactivity.
Formula:C5H12N2
InChI:InChI=1/C5H12N2/c6-5-2-1-3-7-4-5/h5,7H,1-4,6H2/t5-/m1/s1
SMILES:C1C[C@H](CNC1)N
Synonyms:- (3R)-Piperidin-3-amin
- (3R)-Piperidin-3-amine
- 3-piperidinamine, (3R)-
- (R)-piperidin-3-amine
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100
Found 3 products.
(R)-3-Aminopiperidine
CAS:<p>(R)-3-Aminopiperidine is a chiral molecule that can be synthesized by the asymmetric synthesis of benzoic acid. It is a potential hypoglycemic drug and has shown inhibition against DPP-4, which is an enzyme that degrades incretin hormones in the body. The inhibition of DPP-4 may lead to an increase in insulin secretion and it may also have anticancer effects. (R)-3-Aminopiperidine can be used as a starting point for other chemical compounds or pharmaceuticals due to its low cost and availability.</p>Formula:C5H12N2Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:100.16 g/mol
