N-(4-Oxo-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidin-2-yl)acetamide - Names and Identifiers
Name | N-(4-Oxo-1,7-dihydropyrrolo[2,3-d]pyrimidin-2-yl)acetamide
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Synonyms | N-(4-Oxo-1,7-dihydropyrrolo[2,3-d]pyrimidin-2-yl)acetamide N-(4-Oxo-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidin-2-yl)acetamide acetamide, N-(4,7-dihydro-4-oxo-1H-pyrrolo[2,3-d]pyrimidin-2-yl)- Acetamide, N-(4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-2-yl)- N-(5-oxo-2,4,9-triazabicyclo[4.3.0]nona-3,7,10-trien-3-yl)acetamide
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CAS | 62160-25-2
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InChI | InChI=1/C8H8N4O2/c1-4(13)10-8-11-6-5(2-3-9-6)7(14)12-8/h2-3H,1H3,(H3,9,10,11,12,13,14) |
N-(4-Oxo-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidin-2-yl)acetamide - Physico-chemical Properties
Molecular Formula | C8H8N4O2
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Molar Mass | 192.17 |
Density | 1?+-.0.1 g/cm3(Predicted) |
Melting Point | 342-343 °C (decomp) |
pKa | 10.26±0.20(Predicted) |
Refractive Index | 1.758 |
N-(4-Oxo-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidin-2-yl)acetamide - Introduction
N-(4-Oxo-1, 7-dihydrodropyrrolo [2,3-d]pyrimidin-2-yl)acetamide is an organic compound whose chemical formula is C9H10N4O2. The following is a detailed description of its nature, use, preparation and safety information:
Nature:
-Appearance: Colorless or light yellow crystalline solid
-Melting point: about 135-140 degrees Celsius
-Solubility: Soluble in some organic solvents (such as dichloromethane, ethyl acetate), insoluble in water
-Chemical properties: N-(4-Oxo-1, 7-dihydropropyrrolo [2,3-d]pyrimidin-2-yl)acetamide is a compound containing an amide group, which can react with other compounds to form new molecules.
Use:
-Chemical synthesis intermediate: N-(4-Oxo-1, 7-dihydropropyrrolo [2,3-d]pyrimidin-2-yl)acetamide is often used as an intermediate in organic synthesis and can be used to synthesize compounds with different biological activities.
-Drug research: As a compound, it may have potential biological activity, so it may have application prospects in the field of drug research.
Preparation Method:
N-(4-Oxo-1, 7-dihydropropyrrolo [2,3-d]pyrimidin-2-yl)acetamide is prepared by a relatively complicated method and is usually obtained by an organic synthetic route. One possible synthetic method is the oxylation of appropriate precursor compounds to obtain the desired product by a multi-step reaction.
Safety Information:
There is a lack of specific safety information about N-(4-Oxo-1,7-dihydropyrrolo[2,3-d]pyrimidin-2-yl)acetamide. It is recommended to take necessary safety measures when using or handling this compound. Due to its potential biological activity, it must be handled with care and follow appropriate laboratory safety procedures. Wear appropriate personal protective equipment such as laboratory gloves, goggles, and lab coats when using the compound in a laboratory or industrial setting. Also avoid inhalation, contact with skin or ingestion of the compound. In case of accidental exposure or ingestion, seek medical attention immediately. To use this compound, follow the safe practices and recommendations for the chemicals involved.
Last Update:2024-04-09 21:04:16