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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-pyrrolo[2,3-c]pyridine-7-carboxylic acid

OC(=O)c1nccc2c1[nH]cc2 Request for Quotation
Chemical Name: 1H-pyrrolo[2,3-c]pyridine-7-carboxylic acid
CAS Number: 945840-82-4
Product Number: AG00IICY(AGN-PC-09RUXQ)
Synonyms:
MDL No:
Molecular Formula: C8H6N2O2
Molecular Weight: 162.1454

Identification/Properties

Computed Properties
Molecular Weight:
162.148g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
162.043g/mol
Monoisotopic Mass:
162.043g/mol
Topological Polar Surface Area:
66A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
196
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


Utilizing 1H-Pyrrolo[2,3-c]pyridine-7-carboxylic acid in chemical synthesis offers a versatile platform for the construction of structurally complex molecules. This compound can serve as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties. By incorporating this carboxylic acid derivative into synthetic routes, chemists can introduce important functionalities and stereochemical elements into the target molecules, enabling precise control over the desired properties. Its ability to participate in diverse chemical reactions, such as amidation, esterification, and condensation, makes it a valuable tool for the construction of intricate molecular architectures with specific biological or chemical activities. As a strategic intermediate in organic synthesis, 1H-Pyrrolo[2,3-c]pyridine-7-carboxylic acid plays a crucial role in the design and preparation of novel compounds with potential applications across various scientific fields.