99310-57-3 Usage
Explanation
This is the full chemical name of the compound, which helps in identifying its structure and properties.
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms present in the compound.
3. Imidazole Derivative
Explanation
The compound is a derivative of imidazole, which is a five-membered ring containing three carbon atoms, two nitrogen atoms, and one oxygen atom.
4. Pharmaceutical Applications
Explanation
1H-Imidazole-4-propanoic acid, 2,3-dihydro-2-oxohas potential applications in the pharmaceutical industry, possibly as a drug or a key intermediate in drug synthesis.
5. Biological Activities
Explanation
The compound may exhibit various biological activities, such as antimicrobial, antifungal, or antioxidant properties, which could be useful in the development of new treatments or therapies.
6. Organic Chemistry Building Block
Explanation
1H-Imidazole-4-propanoic acid, 2,3-dihydro-2-oxocan be used as a building block in organic chemistry for the synthesis of other compounds, making it a valuable reagent in chemical research and development.
7. Structure
Explanation
The compound consists of a five-membered imidazole ring fused with a propanoic acid chain and a 2,3-dihydro-2-oxo group, which contributes to its unique chemical properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 99310-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,1 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99310-57:
(7*9)+(6*9)+(5*3)+(4*1)+(3*0)+(2*5)+(1*7)=153
153 % 10 = 3
So 99310-57-3 is a valid CAS Registry Number.
99310-57-3Relevant articles and documents
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.
