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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-chloro-2-phenylpyrimidine-4-carboxylic acid

Clc1nc(nc(c1)C(=O)O)c1ccccc1 Request for Quotation
Chemical Name: 6-chloro-2-phenylpyrimidine-4-carboxylic acid
CAS Number: 913952-59-7
Product Number: AG006BH8(AGN-PC-0BTS2Z)
Synonyms:
MDL No:
Molecular Formula: C11H7ClN2O2
Molecular Weight: 234.6385

Identification/Properties

Computed Properties
Molecular Weight:
234.639g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
234.02g/mol
Monoisotopic Mass:
234.02g/mol
Topological Polar Surface Area:
63.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
256
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Chloro-2-phenylpyrimidine-4-carboxylic acid is a versatile compound commonly used in chemical synthesis for its application in the creation of various pharmaceuticals, agrochemicals, and materials. As a key building block in organic chemistry, this compound serves as a crucial intermediate in the synthesis of complex molecules due to its unique structural properties. By incorporating 6-Chloro-2-phenylpyrimidine-4-carboxylic acid into a synthetic route, chemists can introduce specific functionalities and structural motifs that are essential for the desired biological or chemical activity of the final product. Its strategic placement within a molecular framework allows for precise control over the subsequent reactions and transformations, enabling the synthesis of target compounds with high efficiency and selectivity. In the realm of drug discovery and development, this compound plays a vital role in accessing new therapeutic agents with improved efficacy and safety profiles. Additionally, its utility extends to the synthesis of advanced materials with tailored properties for applications in various industrial sectors. Overall, the incorporation of 6-Chloro-2-phenylpyrimidine-4-carboxylic acid in chemical synthesis empowers researchers to construct intricate molecules with enhanced functionality and potential for addressing diverse societal needs.