CAS 3594-37-4

1-(3-Pyridinyl)-1,3-butanedione

Description:

1-(3-Pyridinyl)-1,3-butanedione, also known as 3-Pyridine-1,3-butanedione, is an organic compound characterized by its pyridine ring and a diketone functional group. It features a butanedione backbone with a pyridine substituent at one end, which contributes to its unique chemical properties. This compound typically appears as a yellow to brown solid or liquid, depending on its purity and form. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water due to its hydrophobic nature. The presence of the pyridine ring imparts basicity and potential for coordination with metal ions, making it of interest in coordination chemistry and catalysis. Additionally, its diketone structure allows for various chemical reactions, including condensation and oxidation. 1-(3-Pyridinyl)-1,3-butanedione may also exhibit biological activity, which could be explored for potential applications in pharmaceuticals or agrochemicals. As with many organic compounds, handling should be done with care, considering safety data and potential hazards.

Formula: C₉H₉NO₂

InChI: InChI=1S/C9H9NO2/c1-7(11)5-9(12)8-3-2-4-10-6-8/h2-4,6H,5H2,1H3

InChI key: InChIKey=OVPXWZQQDUKDFN-UHFFFAOYSA-N

SMILES: C(CC(C)=O)(=O)C=1C=CC=NC1

Synonyms:

• 1,3-Butanedione, 1- (3-pyridinyl)-
• 1,3-Butanedione, 1- (3-pyridyl)-
• 1-(3-Pyridinyl)-1,3-butanedione
• 1-(3-Pyridyl)-1,3-butanedione
• 1-Nicotinoylacetone
• NSC 174282
• Nicotinoylacetone

3-Acetoacetylpyridine

CAS: 3594-37-4

Formula: C₉H₉NO₂

Purity: 95%

Molecular weight: 163.1733

Ref: IN-DA007D6T

1-(Pyridin-3-yl)butane-1,3-dione

CAS: 3594-37-4

1-(Pyridin-3-yl)butane-1,3-dione

Purity: 95%

Molecular weight: 163.18g/mol

Ref: 54-OR1002527

1-(Pyridin-3-yl)butane-1,3-dione

CAS: 3594-37-4

Formula: C₉H₉NO₂

Purity: 95%

Molecular weight: 163.176

Ref: 10-F216517

1-(Pyridin-3-yl)butane-1,3-dione

CAS: 3594-37-4

1-(Pyridin-3-yl)butane-1,3-dione is an activating agent that can be used to treat a variety of disorders. It activates the insulin receptor and has been shown to activate the PPAR alpha and gamma heterodimers in vitro. 1-(Pyridin-3-yl)butane-1,3-dione may also have a proliferating effect on cells. This compound is a chelate ring that contains heterocyclic bonds, which are often found in compounds with profiles similar to those of 1-(pyridin-3-yl)butane-1,3-dione. The structural formula for this compound is shown below:

Formula: C₉H₉NO₂

Purity: Min. 95%

Molecular weight: 163.17 g/mol

Ref: 3D-DAA59437