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

Linagliptin EP Impurity J

CAS: 54012-73-6

Formula: C₅H₁₂N₂

Molecular weight: 100.17

Ref: ST-EA-CP-L1095

3-Aminopiperidine

CAS: 54012-73-6

Formula: C₅H₁₂N₂

Purity: 97%

Color and Shape: Liquid

Molecular weight: 100.1622

Ref: IN-DA00DE42

Piperidin-3-amine

CAS: 54012-73-6

Piperidin-3-amine

Purity: 97%

Ref: 54-OR1038682

Alogliptin Impurity 17

CAS: 54012-73-6

Formula: C₅H₁₂N₂

Molecular weight: 100.17

Ref: 4Z-A-4953

3-Aminopiperidine

CAS: 54012-73-6

Formula: C₅H₁₂N₂

Purity: 97%

Color and Shape: Solid, Crystalline

Molecular weight: 100.165

Ref: 10-F064988

3-Aminopiperidine

CAS: 54012-73-6

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: C₅H₁₂N₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 100.16 g/mol

Ref: 3D-FA167658

Alogliptin Impurity 17

CAS: 54012-73-6

Formula: C₅H₁₂N₂

Molecular weight: 100.17

Ref: ST-EA-CP-A13077