1,3-oxazinanes
1,3-Oxazinanes are a class of heterocyclic compounds characterized by the presence of an oxazine ring system, which consists of five atoms: four carbon atoms and one nitrogen atom. Structurally, 1,3-oxazinanes can exist in various forms due to the flexibility of their ring systems, allowing for diverse conformational arrangements. These compounds are widely used in organic synthesis as precursors or intermediates due to their versatile reactivity. They are also of interest in pharmaceutical research because of their potential therapeutic applications, such as acting as inhibitors of various enzymes and being involved in drug transport mechanisms. The stability and reactivity of 1,3-oxazinanes can be tailored by altering the substituents on the ring system, making them valuable tools in synthetic chemistry.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2H-1,3-Oxazine, 3-(dichloroacetyl)tetrahydro- | 71526-29-9 | C6H9Cl2NO2 |
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2H-1,3-Oxazine-2,6(3H)-dione,dihydro- | 5638-70-0 | C4H5NO3 |
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2H-1,3-Oxazine-2-thione,tetrahydro-4,4,6-trimethyl- | 17374-19-5 | C7H13NOS |
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2H-1,3-Oxazin-2-one,tetrahydro-4,4,6-trimethyl- | 27830-77-9 | C7H13NO2 |
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1,3-Oxazinane | 14558-49-7 | C4H9NO |
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1H-Pyrrolo[1,2-c][1,3]oxazine-1-thione, hexahydro-4,5,6,7-tetrahydroxy-, (4S,4aR,5S,6S,7R)- (9CI) | 539020-82-1 | C7H11NO5S |
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54953-80-9 | C5H9NO2 | |
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Cheliensisaminone | 1417919-63-1 | C7H9NO3 |
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2H-1,3-Oxazine-2-thione, tetrahydro-4,4,5,6-tetramethyl- | 125039-11-4 | C8H15NOS |
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5-methyl-1,3-oxazinan-2-one | 100792-01-6 | C5H9NO2 |
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