CAS 10043-37-5

1-(1-Piperidinyl)-2-propen-1-one

Description:

1-(1-Piperidinyl)-2-propen-1-one, also known as piperidinyl acrylaldehyde, is an organic compound characterized by its piperidine ring and an α,β-unsaturated carbonyl group. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It has a molecular formula that reflects its structure, containing both nitrogen and carbonyl functionalities, which contribute to its reactivity. The presence of the piperidine moiety imparts basic properties, allowing it to participate in various chemical reactions, including nucleophilic additions and Michael additions. This compound is of interest in synthetic organic chemistry and may serve as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactivity and structural features make it a valuable building block in the development of more complex molecules. Safety precautions should be observed when handling this substance, as it may pose health risks if inhaled or ingested.

Formula: C₈H₁₃NO

InChI: InChI=1S/C8H13NO/c1-2-8(10)9-6-4-3-5-7-9/h2H,1,3-7H2

InChI key: InChIKey=RESPXSHDJQUNTN-UHFFFAOYSA-N

SMILES: C(C=C)(=O)N1CCCCC1

Synonyms:

• 1-(1-Piperidinyl)-2-propen-1-one
• 1-(2-Propenoyl)piperidine
• 1-Acryloylpiperidine
• 2-Propen-1-One, 1-(1-Piperidinyl)-
• N-Acryloylpiperidine
• N-Pentamethyleneacrylamide
• Piperidine, 1-(1-oxo-2-propenyl)-
• Piperidine, 1-acryloyl-
• 1-(Piperidin-1-yl)prop-2-en-1-one

2-Propen-1-one, 1-(1-piperidinyl)-

CAS: 10043-37-5

Formula: C₈H₁₃NO

Purity: 98%

Color and Shape: Liquid

Molecular weight: 139.1949

Ref: IN-DA0001Z3

1-(Piperidin-1-yl)prop-2-en-1-one

CAS: 10043-37-5

Purity: 98%

Molecular weight: 139.197998

Ref: 10-F690295

1-(Piperidin-1-yl)prop-2-en-1-one

CAS: 10043-37-5

1-(Piperidin-1-yl)prop-2-en-1-one is a heterocycle that is used as a pharmaceutical compound. It is one of the most potent known inhibitors of cellular efflux pumps, which are responsible for recycling natural products and xenobiotics from cells. The inhibition of these pumps by 1-(piperidin-1-yl)prop-2-en-1-one leads to increased concentrations of estrogens in the blood plasma, which has been shown to lead to an increase in breast cancer cell growth. 1-(Piperidin-1-yl)prop-2-en-1-one also inhibits aromatase, an enzyme that converts androgens into estrogens. This can lead to suppression of estrogen levels in males and females. The drug also has depressant activity and is used for treating anxiety disorders.

Formula: C₈H₁₃NO

Purity: Min. 95%

Molecular weight: 139.19 g/mol

Ref: 3D-KAA04337