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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)-

8-Bromopyrido[4,3-d]pyrimidin-4(3H);-one

Brc1cncc2c1nc[nH]c2=O Request for Quotation
Chemical Name: 8-Bromopyrido[4,3-d]pyrimidin-4(3H);-one
CAS Number: 1256353-15-7
Product Number: AG000O37(AGN-PC-0WCZWE)
Synonyms:
MDL No:
Molecular Formula: C7H4BrN3O
Molecular Weight: 226.0302

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The versatile compound 8-Bromopyrido[4,3-d]pyrimidin-4(3H)-one plays a crucial role in chemical synthesis as a key building block in the preparation of various biologically active molecules and pharmaceuticals. Its unique structure and reactivity make it a valuable tool for the creation of novel compounds with potential therapeutic applications. In synthetic chemistry, 8-Bromopyrido[4,3-d]pyrimidin-4(3H)-one serves as a versatile intermediate in the synthesis of complex heterocyclic structures, enabling the efficient assembly of diverse chemical entities. Its presence in the molecular framework imparts desirable properties and functionalities, making it a valuable component for drug discovery and development efforts. In addition, the incorporation of 8-Bromopyrido[4,3-d]pyrimidin-4(3H)-one in chemical reactions can lead to the formation of structurally diverse compounds with enhanced biological activities, thereby offering new possibilities for the exploration of potential therapeutic agents.