1657-34-7

Basic information

• Product Name: 3-oxo-N-(pyridin-3-yl)butanamide
• CAS NO: 1657-34-7
• Molecular Formula: C₉H₁₀N₂O₂
• Molecular Weight: 178.1879
• Mol File: 1657-34-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 393.2°C at 760 mmHg
• Flash Point: 191.6°C
• Density: 1.221g/cm³
• Vapor Pressure: 2.16E-06mmHg at 25°C
• Refractive Index: 1.57
• CAS DataBase Reference: 3-oxo-N-(pyridin-3-yl)butanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-oxo-N-(pyridin-3-yl)butanamide(1657-34-7)
• EPA Substance Registry System: 3-oxo-N-(pyridin-3-yl)butanamide(1657-34-7)

Safety Data

• Hazardous Substances Data: 1657-34-7(Hazardous Substances Data)

Usage

Description

3-oxo-N-(pyridin-3-yl)butanamide is a chemical compound characterized by the molecular formula C10H11NO2. It is an organic compound that features a pyridine ring and a butanamide group. At room temperature, it exists as a yellow solid and exhibits limited solubility in water. 3-oxo-N-(pyridin-3-yl)butanamide is utilized in research and pharmaceutical applications, and it may also serve as a precursor for the synthesis of other organic compounds. Its unique properties and potential applications render it a subject of interest for further study and exploration.

Uses

Used in Pharmaceutical Research:
3-oxo-N-(pyridin-3-yl)butanamide is employed as a research compound for the development of new pharmaceuticals. Its structural features, including the pyridine ring and butanamide group, make it a valuable building block for the synthesis of novel drug candidates.
Used in Organic Synthesis:
In the field of organic chemistry, 3-oxo-N-(pyridin-3-yl)butanamide is used as a starting material for the synthesis of other organic compounds. Its reactivity and functional groups allow for various chemical reactions, leading to the creation of a diverse range of molecules with potential applications in different industries.
Used in Chemical Research:
3-oxo-N-(pyridin-3-yl)butanamide is utilized in chemical research to study the properties and reactivity of compounds containing pyridine rings and amides. This helps in understanding the fundamental principles of organic chemistry and contributes to the advancement of the field.

Upstream product

• 462-08-8 pyridin-3-ylamine 
• 141-97-9 ethyl acetoacetate 
• 5394-63-8 2,2,6-trimethyl-4H-1,3-dioxin-4-one 
• 157562-24-8 3-aminopicolinic acid trimethylsilyl ester 
• 1694-31-1 tert-butyl acetoacetate 
• 157562-25-9 3-(3-oxobutylamido)picolinic acid 
• 1462-86-8 3-amino-pyridine-2-carboxylic acid 

Downstream Products

• 1171116-82-7 4-(1-benzyl-2-(methylthio)-1H-imidazol-5-yl)-2,6-dimethyl-N₃,N₅-bis(pyridin-3-yl)-1,4-dihydropyridine-3,5-dicarboxamide 
• 1171116-76-9 4-(2-(methylthio)-1-(phenylamino)-1H-imidazol-5-yl)-2,6-dimethyl-N₃,N₅-di(pyridin-3-yl)-1,4-dihydropyridine-3,5-dicarboxamide 

Relevant articles and documents

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Activated anilide in heterocyclic synthesis: Synthesis of new dihydropyridines, dihydropyridazines and thiourea derivatives

A series of new dihydropyridines, butanamide, dihydropyridazines and thiourea derivatives have been prepared through the reactions of 3-aminopyridine (1) and N-(pyridin-3-yl)-3-(pyridin-3-ylimino)butanamide 3 with some electrophilic reagents, aryl diazonium salts and isothiocyanates. Elementary analysis, MS, IR, and 1H NMR spectra confirmed the identity of the products. Copyright

Microwave induced acetoacetylation of hetaryl and aryl amines

Acetoacetylation of hetaryl and aryl amines by interaction with ethyl acetoacetate under microwave irradiation, without any catalyst and/or solvent, is reported.