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  2. 2,2-DIMETHYL-6-NITRO-2H-PYRIDO[3,2-B][1,4]OXAZIN-3(4H)-ONE

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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2,2-DIMETHYL-6-NITRO-2H-PYRIDO[3,2-B][1,4]OXAZIN-3(4H)-ONE

O=C1Nc2nc(ccc2OC1(C)C)[N+](=O)[O-] Request for Quotation
Chemical Name: 2,2-DIMETHYL-6-NITRO-2H-PYRIDO[3,2-B][1,4]OXAZIN-3(4H)-ONE
CAS Number: 1002726-59-1
Product Number: AG0001FH(AGN-PC-07CN90)
Synonyms:
MDL No:
Molecular Formula: C9H9N3O4
Molecular Weight: 223.1855

Identification/Properties

Computed Properties
Molecular Weight:
223.188g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
223.059g/mol
Monoisotopic Mass:
223.059g/mol
Topological Polar Surface Area:
97A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
325
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,2-Dimethyl-6-nitro-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one, a versatile compound in chemical synthesis, finds application in various organic reactions due to its unique structure and reactivity. This compound serves as a valuable building block in the synthesis of intricate heterocyclic molecules, pharmaceutical intermediates, and agrochemicals. Its presence enables the introduction of specific functional groups with precision, facilitating the creation of diverse chemical entities. Employed in multi-step organic transformations, 2,2-Dimethyl-6-nitro-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one plays a crucial role in the development of novel synthetic methodologies and the production of compounds with potential biological activities.