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3-Isopropylisoxazolo[5,4-b]pyridine-5-carboxylic acid is a complex organic compound with the molecular formula C10H10N2O2. It belongs to the class of isoxazolopyridine derivatives, which are heterocyclic compounds with potential applications in pharmaceuticals and agrochemicals. This specific compound features a pyridine ring fused to an isoxazole ring, with an isopropyl group attached to the 3-position of the pyridine. The carboxylic acid functional group at the 5-position provides potential sites for further chemical modifications or reactions. Due to its unique structure, 3-isopropylisoxazolo[5,4-b]pyridine-5-carboxylic acid may exhibit interesting biological activities, making it a subject of interest for researchers in the field of drug discovery and development.

2372-49-8

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2372-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2372-49-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,7 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2372-49:
(6*2)+(5*3)+(4*7)+(3*2)+(2*4)+(1*9)=78
78 % 10 = 8
So 2372-49-8 is a valid CAS Registry Number.

2372-49-8Relevant academic research and scientific papers

Ammonium Chloride-Promoted Rapid Synthesis of Monosubstituted Ureas under Microwave Irradiation

Lan, Chunling Blue,Auclair, Karine

supporting information, p. 5135 - 5146 (2021/10/19)

Monosubstituted ureas are important scaffolds in organic chemistry. They appear in various biologically active compounds and serve as versatile precursors in synthesis. Monosubstituted ureas were originally prepared using toxic and hazardous phosgene equivalents. Modern methods include transamidation of urea and nucleophilic addition to cyanate salts, both of which suffer from a narrow substrate scope due to the need for a strong acid and prolonged reaction times. We hereby report that ammonium chloride can promote the reaction between amines and potassium cyanate to generate monosubstituted ureas in water. This method proceeds rapidly under microwave irradiation and tolerates a broad range of functional groups. Unlike previous strategies, it is compatible with other nucleophiles, acid-labile moieties, and most of the common protecting groups. The products precipitate out of solution, allowing facile isolation without column chromatography.

A practically simple, catalyst free and scalable synthesis of: N -substituted ureas in water

Tiwari, Lata,Kumar, Varun,Kumar, Bhuvesh,Mahajan, Dinesh

, p. 21585 - 21595 (2018/06/26)

A practically simple, mild and efficient method is developed for the synthesis of N-substituted ureas by nucleophilic addition of amines to potassium isocyanate in water without organic co-solvent. Using this methodology, a variety of N-substituted ureas (mono-, di- and cyclic-) were synthesized in good to excellent yields with high chemical purity by applying simple filtration or routine extraction procedures avoiding silica gel purification. The developed methodology was also found to be suitable for gram scale synthesis of molecules having commercial application in large volumes. The identified reaction conditions were found to promote a unique substrate selectivity from a mixture of two amines.

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