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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)-

3-Pyridinecarboxylic acid, 6-(1H-pyrrol-1-yl)-

OC(=O)c1ccc(nc1)n1cccc1 Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 6-(1H-pyrrol-1-yl)-
CAS Number: 175135-86-1
Product Number: AG00ALZK(AGN-PC-0KKPZY)
Synonyms:
MDL No:
Molecular Formula: C10H8N2O2
Molecular Weight: 188.1827

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-(1H-Pyrrol-1-yl)nicotinic acid, also known as $name$, serves as a versatile building block in chemical synthesis. This compound is commonly utilized as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure, $name$ offers a wide range of functionalization possibilities, making it a valuable tool for organic chemists.In chemical synthesis, $name$ can be used to introduce the 1H-pyrrol-1-yl and nicotinic acid moieties into target molecules, enabling the creation of new compounds with tailored properties. Its reactivity allows for the formation of complex molecular structures through various synthetic routes, such as functional group transformations, cross-coupling reactions, and heterocyclic ring formations.Moreover, the presence of the pyrrole ring in $name$ confers specific biological activities to the resulting compounds, making it particularly valuable in medicinal chemistry research. By incorporating 6-(1H-Pyrrol-1-yl)nicotinic acid into drug candidates, researchers can explore new ways to modulate biological targets and develop novel therapeutics for a wide range of diseases.Overall, the strategic use of 6-(1H-Pyrrol-1-yl)nicotinic acid in chemical synthesis allows for the efficient and precise construction of diverse molecular architectures with potential applications in the fields of pharmaceuticals, agrochemicals, and materials science.