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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)-

Furo[2,3-c]pyridine-2-carboxylic acid

OC(=O)c1cc2c(o1)cncc2 Request for Quotation
Chemical Name: Furo[2,3-c]pyridine-2-carboxylic acid
CAS Number: 112372-15-3
Product Number: AG008UA7(AGN-PC-00O1ZF)
Synonyms:
MDL No:
Molecular Formula: C8H5NO3
Molecular Weight: 163.1302

Identification/Properties

Computed Properties
Molecular Weight:
163.132g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
163.027g/mol
Monoisotopic Mass:
163.027g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
195
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


Furo[2,3-c]pyridine-2-carboxylic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure makes it a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and organic materials.In the realm of chemical synthesis, $name$ serves as an important precursor in the creation of heterocyclic compounds. Its distinct furo[2,3-c]pyridine core provides a strategic starting point for the construction of more complex molecules through functional group manipulation and diversification.Researchers and chemists frequently utilize $name$ as a key intermediate in the synthesis of bioactive compounds due to its potential to impart desired biological properties. By incorporating this compound into synthetic pathways, chemists can access a diverse array of derivatives with enhanced pharmacological activities.$name$ plays a crucial role in the development of novel drug candidates, agrochemicals, and advanced materials by enabling the efficient synthesis of structurally intricate molecules. Its functional versatility and synthetic utility make it a valuable asset in the toolkit of synthetic chemists aiming to construct innovative compounds with tailored properties.