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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)-

6,7-dihydro-5H-cyclopenta[b]pyridine-4-carboxylic acid

OC(=O)c1ccnc2c1CCC2 Request for Quotation
Chemical Name: 6,7-dihydro-5H-cyclopenta[b]pyridine-4-carboxylic acid
CAS Number: 953428-98-3
Product Number: AG00IIZZ(AGN-PC-0ALRR8)
Synonyms:
MDL No:
Molecular Formula: C9H9NO2
Molecular Weight: 163.17326

Identification/Properties

Computed Properties
Molecular Weight:
163.176g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
163.063g/mol
Monoisotopic Mass:
163.063g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
193
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6,7-Dihydro-5H-cyclopenta[b]pyridine-4-carboxylic acid is a versatile compound widely used in chemical synthesis as a key building block for the creation of various pharmaceuticals and agrochemicals. This compound serves as a crucial intermediate in the synthesis of biologically active compounds due to its unique structural features and reactivity. Its cyclic structure provides a solid foundation for creating complex molecules with specific biological activities.In chemical synthesis, 6,7-Dihydro-5H-cyclopenta[b]pyridine-4-carboxylic acid can be utilized as a precursor for the synthesis of diverse heterocyclic compounds through functional group transformations and derivatizations. Its carboxylic acid functionality allows for further modification through coupling reactions, enabling the introduction of additional substituents or functional groups to tailor the properties of the final product.Moreover, the presence of a pyridine ring in the structure of this compound imparts specific chemical reactivity, making it a valuable component in the construction of pharmacologically relevant molecules such as antiviral agents, antimicrobial compounds, and enzyme inhibitors. By leveraging the synthetic capabilities of 6,7-Dihydro-5H-cyclopenta[b]pyridine-4-carboxylic acid, chemists can access a wide range of bioactive compounds with potential therapeutic applications.