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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)-

1H-Imidazo[4,5-b]pyridine-2-carboxylic acid

OC(=O)c1nc2c([nH]1)nccc2 Request for Quotation
Chemical Name: 1H-Imidazo[4,5-b]pyridine-2-carboxylic acid
CAS Number: 97640-15-8
Product Number: AG006BPM(AGN-PC-03R724)
Synonyms:
MDL No:
Molecular Formula: C7H5N3O2
Molecular Weight: 163.1335

Identification/Properties

Properties
BP:
391.1±25.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
163.136g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
163.038g/mol
Monoisotopic Mass:
163.038g/mol
Topological Polar Surface Area:
78.9A^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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3H-Imidazo[4,5-b]pyridine-2-carboxylic acid is a versatile compound that finds extensive applications in chemical synthesis. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials. This compound is particularly valued for its ability to participate in diverse reactions such as cross-coupling, cycloaddition, and condensation processes. In the context of chemical synthesis, 3H-Imidazo[4,5-b]pyridine-2-carboxylic acid acts as a valuable intermediate, enabling the construction of intricate molecular structures with precision and efficiency. Its strategic incorporation in synthetic routes contributes significantly to the synthesis of novel compounds with enhanced properties and functionalities.