7-chloro-1H-pyrido[2,3-d]pyrimidine-2,4-dione|938443-19-7,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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-chloro-1H-pyrido[2,3-d]pyrimidine-2,4-dione

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Chemical Name:	7-chloro-1H-pyrido[2,3-d]pyrimidine-2,4-dione
CAS Number:	938443-19-7
Product Number:	AG005ZW7(AGN-PC-05VCHB)
Synonyms:
MDL No:
Molecular Formula:	C7H4ClN3O2
Molecular Weight:	197.5786

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Identification/Properties

Properties

Storage:

2-8℃;Light sensitive;

Form:

Solid

Safety Information

GHS Pictogram:

N/A

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Chemical Structure

7-Chloropyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione serves as a valuable building block in chemical synthesis processes, particularly in the pharmaceutical and agrochemical industries. This compound exhibits unique reactivity that lends itself well to the formation of various heterocyclic compounds with diverse functionalities. Its versatile nature allows for the introduction of specific chemical groups and modifications, making it a key intermediate in the synthesis of bioactive molecules and drug candidates. This compound is commonly employed in the design and development of new therapeutic agents, offering a strategic starting point for the creation of novel compounds with potential pharmacological applications.