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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)-

2H-Pyrido[3,2-b]-1,4-oxazin-3(4H)-one, 2,2-dimethyl-

O=C1Nc2ncccc2OC1(C)C Request for Quotation
Chemical Name: 2H-Pyrido[3,2-b]-1,4-oxazin-3(4H)-one, 2,2-dimethyl-
CAS Number: 20348-21-4
Product Number: AG0028WP(AGN-PC-0JLXGY)
Synonyms:
MDL No:
Molecular Formula: C9H10N2O2
Molecular Weight: 178.1879

Identification/Properties

Computed Properties
Molecular Weight:
178.191g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
178.074g/mol
Monoisotopic Mass:
178.074g/mol
Topological Polar Surface Area:
51.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
228
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,2-Dimethyl-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one, also known as $name$, is a versatile compound widely utilized in chemical synthesis. With its unique structure and reactivity, this compound serves as a valuable building block for the preparation of various organic molecules. In organic synthesis, $name$ can undergo a range of functional group transformations, such as acylation, alkylation, and cyclization reactions, enabling the construction of complex molecular structures. Additionally, the nitrogen-containing heterocyclic framework of $name$ makes it particularly useful in the development of pharmaceuticals, agrochemicals, and other bioactive compounds. Its ability to participate in diverse chemical reactions and form key intermediates highlights its significance as a valuable tool in the synthesis of novel organic substances.