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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)-

6-amino-5-chloropyrimidine-4-carboxylic acid

OC(=O)c1ncnc(c1Cl)N Request for Quotation
Chemical Name: 6-amino-5-chloropyrimidine-4-carboxylic acid
CAS Number: 914916-98-6
Product Number: AG0069UT(AGN-PC-0BS6OL)
Synonyms:
MDL No:
Molecular Formula: C5H4ClN3O2
Molecular Weight: 173.5572

Identification/Properties

Properties
Storage:
Light sensitive;Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
173.556g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
172.999g/mol
Monoisotopic Mass:
172.999g/mol
Topological Polar Surface Area:
89.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
166
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Amino-5-chloro-4-pyrimidinecarboxylic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block in the creation of various compounds. This chemical compound is widely utilized in the pharmaceutical industry for the synthesis of novel drugs and active pharmaceutical ingredients (APIs). Its unique structure and reactivity make it a valuable intermediate in the creation of diverse pharmaceutical compounds.In chemical synthesis, $name$ is often used as a key starting material for the preparation of heterocyclic compounds, which are essential components of many drug molecules. Its amino and chloro functional groups allow for selective modifications, enabling chemists to tailor the structure of the final compound to achieve specific properties or biological activities.Moreover, $name$ serves as a key intermediate in the synthesis of agrochemicals, dyes, and other specialty chemicals. Its ability to undergo various chemical transformations makes it a versatile building block for organic synthesis, enabling the creation of complex molecules with specific functionalities. By leveraging the unique properties of $name$, chemists can access a wide range of structurally diverse compounds that find applications in various industries.Overall, the strategic utilization of 6-Amino-5-chloro-4-pyrimidinecarboxylic acid in chemical synthesis enables researchers and chemists to access new and innovative compounds with potential applications in drug discovery, material science, and other fields of research.