CAS 50541-93-0

4-Amino-1-benzylpiperidine

Description:

4-Amino-1-benzylpiperidine is an organic compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The presence of an amino group at the 4-position and a benzyl group at the 1-position contributes to its unique chemical properties. This compound is typically a white to off-white solid and is soluble in polar organic solvents. It exhibits basic properties due to the amino group, allowing it to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. 4-Amino-1-benzylpiperidine is of interest in medicinal chemistry and pharmacology, as it may serve as a precursor or intermediate in the synthesis of biologically active compounds. Its potential applications include research in neuropharmacology and the development of new therapeutic agents. However, safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity and reactivity.

Formula: C₁₂H₁₈N₂

InChI: InChI=1S/C12H18N2/c13-12-6-8-14(9-7-12)10-11-4-2-1-3-5-11/h1-5,12H,6-10,13H2

InChI key: InChIKey=YUBDLZGUSSWQSS-UHFFFAOYSA-N

SMILES: C(N1CCC(N)CC1)C2=CC=CC=C2

Synonyms:

• (1-Benzylpiperidin-4-yl)amine
• 1-(Phenylmethyl)-4-piperidinamine
• 1-(Phenylmethyl)-4-piperidinamine, Base Form
• 1-Benzyl-4-Aminopiperidine
• 1-Benzyl-4-piperidinamine
• 1-Benzyl-4-piperidinylamine
• 1-Benzyl-piperidin-4-ylamine
• 1-Benzylpiperidin-4-amine
• 1-Benzylpiperidine-4-amine
• 2-Amino-1-benzylpiperidine
• 4-(1-Piperidinylmethyl)aniline
• 4-(Piperidin-1-Ylmethyl)Aniline
• 4-(Piperidin-1-Ylmethyl)Benzenamine
• 4-Amino-1-(phenylmethyl)piperidine
• 4-Amino-1-Benzyl Piperidine
• 4-Amino-1-benzylpiperdine
• 4-Amino-N-benzylpiperidine
• 4-Piperidin-1-Ylmethyl-Phenylamine
• 4-Piperidinamine, 1-(phenylmethyl)-
• N-Benzyl-4-Amino Piperidine
• N-Benzyl-4-aminopiperidine
• N-Benzyl-4-piperidinamine
• N-benzyl-4-piperidylamine
• N-benzylpiperidin-4-amine

4-Amino-1-benzylpiperidine

CAS: 50541-93-0

Formula: C₁₂H₁₈N₂

Purity: 96%

Color and Shape: Liquid

Molecular weight: 190.2847

Ref: IN-DA003KNI

Clebopride EP Impurity B

CAS: 50541-93-0

Formula: C₁₂H₁₈N₂

Molecular weight: 190.29

Ref: 4Z-C-457003

4-Amino-1-benzylpiperidine

CAS: 50541-93-0

Formula: C₁₂H₁₈N₂

Molecular weight: 190.29

Ref: 7W-GL3167

4-Amino-1-benzylpiperidine

CAS: 50541-93-0

Formula: C₁₂H₁₈N₂

Purity: >98.0%(GC)(T)

Color and Shape: Colorless to Light yellow to Light orange clear liquid

Molecular weight: 190.29

Ref: 3B-A1086

1-(Phenylmethyl)-4-piperidinamine

Controlled Product

CAS: 50541-93-0

Applications 1-(Phenylmethyl)-4-piperidinamine is used in the preparation of 4-substituted coumarins as novel acetylcholinesterase inhibitors used in the treatment and various therapeutic approaches to Alzheimer’s disease. It is also used in the synthesis of nicotinamide derivatives as anti-angiogenic agents.
References Razavi, S. et al.: Eur. J. Med. Chem., 64, 252 (2013); Choi, H. et al.: Bioorg. Med. Chem. Lett., 23, 2083 (2013);

Formula: C₁₂H₁₈N₂

Color and Shape: Neat

Molecular weight: 190.28

Ref: TR-P335840

4-Amino-1-benzylpiperidine

Controlled Product

CAS: 50541-93-0

4-Amino-1-benzylpiperidine is a molecule that has potent inhibitory activity against bladder cancer cells. It also has inhibitory effects on tyrosinase and histone lysine methyltransferase activities, which are enzymes important in the production of melanin and amyloid proteins. 4-Amino-1-benzylpiperidine is a benzyl derivative with radical scavenging activities, which may be due to its ability to react with free radicals. This drug is being researched for its potential use as a therapeutic agent for the treatment of bladder cancer, Alzheimer's disease, and other conditions.

Formula: C₁₂H₁₈N₂

Purity: Min. 97.5 Area-%

Color and Shape: Clear Liquid

Molecular weight: 190.28 g/mol

Ref: 3D-FA11173

4-Amino-1-benzylpiperidine

CAS: 50541-93-0

Formula: C₁₂H₁₈N₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 190.29

Ref: 10-F008925