CAS 54012-73-6
:(+/-)3-Amino piperidine
Description:
(+/-)3-Amino piperidine, with the CAS number 54012-73-6, is a bicyclic organic compound characterized by a piperidine ring with an amino group attached at the 3-position. This compound exists as a racemic mixture, meaning it contains equal parts of two enantiomers, which can exhibit different biological activities. The presence of the amino group contributes to its basicity and potential reactivity, making it a useful intermediate in organic synthesis and pharmaceutical development. The piperidine ring structure provides a degree of rigidity, influencing the compound's conformational properties and interactions with biological targets. Additionally, (+/-)3-amino piperidine may participate in hydrogen bonding due to the amino group, enhancing its solubility in polar solvents. Its applications can range from serving as a building block in the synthesis of more complex molecules to potential roles in medicinal chemistry, particularly in the development of drugs targeting the central nervous system. As with many amines, it is important to handle this compound with care, considering its potential reactivity and the need for proper safety protocols in laboratory settings.
Formula:C5H12N2
InChI:InChI=1/C5H12N2/c6-5-2-1-3-7-4-5/h5,7H,1-4,6H2
SMILES:C1CC(CNC1)N
Synonyms:- 3-Aminopiperidine
- Piperidin-3-Amine
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Found 9 products.
3-Aminopiperidine
CAS:Formula:C5H12N2Purity:97%Color and Shape:Solid, CrystallineMolecular weight:100.1653-Aminopiperidine
CAS:3-Aminopiperidine is an amine that can be synthesized by the reaction of trifluoroacetic acid and hydrochloric acid with primary amines. 3-Aminopiperidine inhibits the enzyme catalysis of aromatic hydrocarbons, which are a precursor to the formation of aryl halides. These reactions are catalyzed by an enzyme called nitrile hydratase. 3-Aminopiperidine has been shown to have therapeutic effects on inflammatory diseases such as rheumatoid arthritis, asthma, and ulcerative colitis. The drug also exhibits anti-inflammatory properties that may be due to its ability to inhibit prostaglandin synthesis.Formula:C5H12N2Purity:Min. 95%Color and Shape:PowderMolecular weight:100.16 g/mol
