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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)-

5-Chloro-6-oxo-1,6-dihydropyrimidine-4-carboxylic acid

OC(=O)c1nc[nH]c(=O)c1Cl Request for Quotation
Chemical Name: 5-Chloro-6-oxo-1,6-dihydropyrimidine-4-carboxylic acid
CAS Number: 914916-96-4
Product Number: AG00IGQ5(AGN-PC-0WAHT9)
Synonyms:
MDL No:
Molecular Formula: C5H3ClN2O3
Molecular Weight: 174.54192

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Chloro-6-oxo-1,6-dihydropyrimidine-4-carboxylic acid, also known by its chemical formula C6H4ClNO3, plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly used as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it a valuable starting material in the synthesis of complex organic compounds.One of the main applications of 5-Chloro-6-oxo-1,6-dihydropyrimidine-4-carboxylic acid is its involvement in the synthesis of pyrimidine derivatives, which are important structural motifs found in many biologically active molecules. By utilizing this compound as a starting material, chemists can access a wide range of pyrimidine-based compounds with diverse pharmacological activities.Furthermore, 5-Chloro-6-oxo-1,6-dihydropyrimidine-4-carboxylic acid can be employed in the synthesis of nucleoside analogs, which are key components in the development of antiviral and anticancer drugs. Through strategic functional group transformations and chemical modifications, this compound can be tailored to introduce specific functionalities into the final product, allowing for the creation of novel compounds with enhanced biological activities.In addition, 5-Chloro-6-oxo-1,6-dihydropyrimidine-4-carboxylic acid serves as a valuable substrate in transition metal-catalyzed reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds in a controlled and efficient manner. This versatility in chemical reactivity makes it a highly sought-after compound in the field of organic synthesis, offering a platform for exploring new synthetic methodologies and expanding the toolkit available to synthetic chemists.