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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)-

7-bromo-2,4-dihydro-1H-pyrido[2,3-b]pyrazin-3-one

O=C1CNc2c(N1)ncc(c2)Br Request for Quotation
Chemical Name: 7-bromo-2,4-dihydro-1H-pyrido[2,3-b]pyrazin-3-one
CAS Number: 957198-15-1
Product Number: AG006BKT(AGN-PC-0CAADI)
Synonyms:
MDL No:
Molecular Formula: C7H6BrN3O
Molecular Weight: 228.0460

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
228.049g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
226.969g/mol
Monoisotopic Mass:
226.969g/mol
Topological Polar Surface Area:
54A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
199
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Bromo-1,2-dihydropyrido[2,3-b]pyrazin-3(4H)-one is a versatile compound that plays a crucial role in chemical synthesis as a key building block. Its unique structure and reactivity make it particularly valuable in the production of a wide range of advanced materials and pharmaceutical intermediates. In chemical synthesis, this compound serves as a valuable starting material for the synthesis of various heterocyclic compounds with diverse biological activities. Its presence in the reaction mixture allows for the formation of complex molecular structures through a series of well-defined chemical transformations. Additionally, the strategic incorporation of 7-Bromo-1,2-dihydropyrido[2,3-b]pyrazin-3(4H)-one in the design of novel synthetic routes enables chemists to access diverse molecular scaffolds with enhanced properties. Its application in chemical synthesis underscores its significance as a key player in the development of innovative compounds with potential applications in drug discovery and materials science.