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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)-

4-Pyrimidinecarboxylic acid, 5-chloro-2-(4-morpholinyl)-

OC(=O)c1nc(ncc1Cl)N1CCOCC1 Request for Quotation
Chemical Name: 4-Pyrimidinecarboxylic acid, 5-chloro-2-(4-morpholinyl)-
CAS Number: 327064-07-3
Product Number: AG00I688(AGN-PC-0KETEQ)
Synonyms:
MDL No:
Molecular Formula: C9H10ClN3O3
Molecular Weight: 243.6470

Identification/Properties

Computed Properties
Molecular Weight:
243.647g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
243.041g/mol
Monoisotopic Mass:
243.041g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
260
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


5-Chloro-2-(4-morpholinyl)-4-pyrimidinecarboxylic acid is a versatile compound widely utilized in chemical synthesis processes. This compound serves as a key building block in the creation of pharmaceuticals, agrochemicals, and other fine chemicals. With its unique structural properties, it can be efficiently modified and functionalized to produce a diverse range of derivatives with specific properties and applications. In organic synthesis, this compound plays a crucial role as a starting material for the preparation of various biologically active compounds and intermediates. Its compatibility with a wide range of reaction conditions and its ability to undergo multiple types of chemical transformations make it an essential component in the toolbox of synthetic chemists. Whether it is used in developing new drug candidates or in designing novel materials, 5-Chloro-2-(4-morpholinyl)-4-pyrimidinecarboxylic acid remains a valuable asset in the realm of chemical synthesis.