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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)-

1,2,4-Triazolo[4,3-a]pyridine-6-carboxylicacid

OC(=O)c1ccc2n(c1)cnn2 Request for Quotation
Chemical Name: 1,2,4-Triazolo[4,3-a]pyridine-6-carboxylicacid
CAS Number: 933708-92-0
Product Number: AG00H0EN(AGN-PC-078TOT)
Synonyms:
MDL No:
Molecular Formula: C7H5N3O2
Molecular Weight: 163.1335

Identification/Properties

Computed Properties
Molecular Weight:
163.136g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
163.038g/mol
Monoisotopic Mass:
163.038g/mol
Topological Polar Surface Area:
67.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
197
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


[1,2,4]Triazolo[4,3-a]pyridine-6-carboxylic acid is a versatile compound widely employed in chemical synthesis as a key building block for the creation of diverse classes of organic molecules. Its unique molecular structure confers specific chemical reactivity and functionality that make it valuable in various synthetic pathways.This compound is commonly utilized in the synthesis of heterocyclic compounds, pharmaceuticals, agrochemicals, and advanced materials. Its incorporation in the chemical synthesis process allows for the introduction of the [1,2,4]Triazolo[4,3-a]pyridine moiety into the target molecules, thereby imparting specific properties and functionalities.In organic synthesis, [1,2,4]Triazolo[4,3-a]pyridine-6-carboxylic acid serves as a precursor for the preparation of novel compounds with potential biological activities and industrial applications. Its versatility and compatibility with various reaction conditions make it a valuable tool for chemists seeking to access complex and structurally diverse molecules in a controlled and efficient manner.Its role as a chemical intermediate in the synthesis of biologically active compounds highlights its importance in drug discovery and development. By incorporating [1,2,4]Triazolo[4,3-a]pyridine-6-carboxylic acid into the molecular design of pharmaceutical candidates, researchers can explore new avenues for the treatment of diseases and disorders.Overall, the strategic use of [1,2,4]Triazolo[4,3-a]pyridine-6-carboxylic acid in chemical synthesis enables the creation of novel molecules with tailored properties and functionalities, making it an indispensable tool for organic chemists and researchers across various scientific disciplines.