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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)-

5H-Thiazolo[3,2-a]pyrimidine-6-carboxylic acid, 2,3-dihydro-5-oxo-

OC(=O)c1cnc2n(c1=O)CCS2 Request for Quotation
Chemical Name: 5H-Thiazolo[3,2-a]pyrimidine-6-carboxylic acid, 2,3-dihydro-5-oxo-
CAS Number: 32084-55-2
Product Number: AG007HEJ(AGN-PC-0K9A3N)
Synonyms:
MDL No:
Molecular Formula: C7H6N2O3S
Molecular Weight: 198.1991

Identification/Properties

Computed Properties
Molecular Weight:
198.196g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
198.01g/mol
Monoisotopic Mass:
198.01g/mol
Topological Polar Surface Area:
95.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
348
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-Oxo-3,5-dihydro-2H-thiazolo[3,2-a]pyrimidine-6-carboxylic acid is a versatile compound commonly utilized in chemical synthesis for the development of novel pharmaceuticals and agrochemicals. This compound serves as a crucial building block in the creation of various heterocyclic structures, owing to its unique thiazolo-pyrimidine core. Its functional groups enable efficient manipulation of its chemical properties, making it an essential component in the construction of diverse molecular architectures. Furthermore, the presence of the carboxylic acid moiety facilitates derivatization, allowing for the introduction of specific functionalities to tailor the compound for desired applications. In the realm of chemical synthesis, 5-Oxo-3,5-dihydro-2H-thiazolo[3,2-a]pyrimidine-6-carboxylic acid plays a pivotal role in the strategic design and assembly of complex organic molecules with potential biological activities.