77727-88-9

Basic information

• Product Name: pyridin-3-yl(pyrrolidin-1-yl)methanone
• CAS NO: 77727-88-9
• Molecular Formula: C₁₀H₁₂N₂O
• Molecular Weight: 176.2151
• Mol File: 77727-88-9.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 328.8°C at 760 mmHg
• Flash Point: 152.6°C
• Density: 1.174g/cm³
• Vapor Pressure: 0.000186mmHg at 25°C
• Refractive Index: 1.577
• CAS DataBase Reference: pyridin-3-yl(pyrrolidin-1-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: pyridin-3-yl(pyrrolidin-1-yl)methanone(77727-88-9)
• EPA Substance Registry System: pyridin-3-yl(pyrrolidin-1-yl)methanone(77727-88-9)

Safety Data

• Hazardous Substances Data: 77727-88-9(Hazardous Substances Data)

Upstream product

• 123-75-1 pyrrolidine 
• 59-67-6 nicotinic acid 
• 614-18-6 3-pyridinecarboxylic acid ethyl ester 
• 20260-53-1 pyridine-3-carbonyl chloride hydrochloride 
• 10400-19-8 3-pyridinecarbonyl chloride 
• 500-22-1 3-pyridinecarboxaldehyde 

Downstream Products

• 101715-40-6 1-phenethyl-piperidine-3-carboxylic acid pyrrolidide 
• 370-09-2 N-(3-pyridylmethyl)pyrrolidine 
• 5424-19-1 3-Benzoylpyridine 
• 21327-72-0 pyridin-3-yl(thiophen-2-yl)methanone 

Relevant articles and documents

Amide Bond Formation via Aerobic Photooxidative Coupling of Aldehydes with Amines Catalyzed by a Riboflavin Derivative

We report an effective, operationally simple, and environmentally friendly system for the synthesis of tertiary amides by the oxidative coupling of aromatic or aliphatic aldehydes with amines mediated by riboflavin tetraacetate (RFTA), an inexpensive organic photocatalyst, and visible light using oxygen as the sole oxidant. The method is based on the oxidative power of an excited flavin catalyst and the relatively low oxidation potential of the hemiaminal formed by amine to aldehyde addition.

Method for preparing amide compound by photocatalysis of nitrogen-containing heterocyclic compound

The invention provides a method for preparing an amide compound by photocatalysis of a nitrogen-containing heterocyclic compound. The method comprises the following steps: mixing the nitrogen-containing heterocyclic compound, organic carboxylic acid and tetrahalomethane in a solvent, adding a catalyst, and reacting under the illumination condition to prepare the amide compound. According to the invention, the organic carboxylic acid, the nitrogen-containing heterocyclic compound containing reactive hydrogen on nitrogen atoms and the tetrahalomethane are used as raw materials, so the raw materials are wide in source, low in cost and high in safety, and large-scale production is facilitated; the halogen simple substance is co-produced in the reaction process, the added value is high, a large amount of waste is prevented from being generated, and the method has high atom economy and environmental friendliness; light conditions are adopted to replace traditional heating and high-pressure conditions, the reaction conditions are mild, environmental pollution is reduced, and the reaction cost is reduced; the method has the advantages of good substrate applicability, mild process conditions, environmental protection, simple process, simple and feasible operation method, and facilitation of popularization and application.

Synthesis of Ag/g-C3N4Composite as Highly Efficient Visible-Light Photocatalyst for Oxidative Amidation of Aromatic Aldehydes

In this contribution, an Ag/g-C3N4nanocomposite was synthesized and utilized as highly efficient and green photocatalyst for organic reactions under visible light irradiation. A layered, porous g-C3N4was synthes