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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)-

4-(1H-Pyrrol-1-yl)pyridine-2-carboxylic acid

OC(=O)c1nccc(c1)n1cccc1 Request for Quotation
Chemical Name: 4-(1H-Pyrrol-1-yl)pyridine-2-carboxylic acid
CAS Number: 887206-82-8
Product Number: AG019Z9U(AGN-PC-0WCN3N)
Synonyms:
MDL No: MFCD04971956
Molecular Formula: C10H8N2O2
Molecular Weight: 188.1827

Identification/Properties

Computed Properties
Molecular Weight:
188.186g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
188.059g/mol
Monoisotopic Mass:
188.059g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
214
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


4-(1H-Pyrrol-1-yl)pyridine-2-carboxylic acid is a versatile molecule widely used in chemical synthesis as a building block for various pharmaceutical and organic compounds. It serves as a key intermediate in the synthesis of heterocyclic compounds and drug molecules due to its unique structural features and reactivity.This compound plays a crucial role in the development of new drugs and therapeutic agents. Its functional groups enable it to participate in various reactions such as cyclization, condensation, and substitution, leading to the formation of complex molecular structures with specific biological activities. In medicinal chemistry, this compound is often employed in the synthesis of pyridine derivatives and other bioactive compounds with potential pharmacological properties.Furthermore, 4-(1H-Pyrrol-1-yl)pyridine-2-carboxylic acid is utilized in the preparation of novel materials with advanced properties, including polymers, dyes, and catalysts. Its strategic placement of functional groups allows for precise control over the chemical modification of the molecule, enabling the tailoring of its properties for specific applications.Overall, the versatile nature of 4-(1H-Pyrrol-1-yl)pyridine-2-carboxylic acid makes it an indispensable building block in chemical synthesis, playing a vital role in advancing the fields of pharmaceuticals, materials science, and organic chemistry.