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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-bromo-[1,2,4]triazolo[4,3-a]pyridine-3-carboxylic acid

Brc1ccc2n(c1)c(nn2)C(=O)O Request for Quotation
Chemical Name: 6-bromo-[1,2,4]triazolo[4,3-a]pyridine-3-carboxylic acid
CAS Number: 1159831-86-3
Product Number: AG000HD4(AGN-PC-0J0Y52)
Synonyms:
MDL No:
Molecular Formula: C7H4BrN3O2
Molecular Weight: 242.0296

Identification/Properties

Computed Properties
Molecular Weight:
242.032g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
240.949g/mol
Monoisotopic Mass:
240.949g/mol
Topological Polar Surface Area:
67.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
226
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-[1,2,4]triazolo[4,3-a]pyridine-3-carboxylic acid is a versatile chemical compound that finds significant application in chemical synthesis processes. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structure and reactivity. By incorporating 6-Bromo-[1,2,4]triazolo[4,3-a]pyridine-3-carboxylic acid into synthetic pathways, chemists can introduce specific functional groups and structural motifs with precision, enabling the efficient production of complex molecules. Its presence can lead to the formation of diverse heterocyclic compounds, which are essential in drug discovery and materials science. Additionally, the incorporation of this compound into organic frameworks can enhance the biological activity or physical properties of the resulting molecules, making it a valuable tool for chemical researchers seeking to design novel compounds for various applications.