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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)-

Cyclopentanecarboxylic acid, 1-(4-aminophenyl)-

OC(=O)C1(CCCC1)c1ccc(cc1)N Request for Quotation
Chemical Name: Cyclopentanecarboxylic acid, 1-(4-aminophenyl)-
CAS Number: 91640-63-0
Product Number: AG00GSC0(AGN-PC-0LFEPZ)
Synonyms:
MDL No:
Molecular Formula: C12H15NO2
Molecular Weight: 205.2530

Identification/Properties

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


1-(4-Aminophenyl)cyclopentanecarboxylic acid, also known as $name$, is a versatile compound widely used in chemical synthesis, particularly in the pharmaceutical industry. This compound serves as a key building block for the synthesis of various biologically active molecules, including pharmaceutical drugs and agrochemicals. Its unique structure and reactivity make it a valuable intermediate in the preparation of a wide range of organic compounds.In chemical synthesis, $name$ is often utilized as a precursor for the synthesis of heterocyclic compounds, which are essential in the development of new drugs and materials. By functionalizing the amine and carboxylic acid groups present in $name$, chemists can introduce new chemical functionalities and create complex molecular structures with tailored properties. This enables the synthesis of diverse pharmacophores and drug candidates with enhanced biological activities and specific target interactions.Furthermore, the cyclopentane ring in $name$ provides rigidity and stereochemical control, making it a valuable scaffold for designing chiral molecules and pharmaceutical agents. Through strategic modifications and transformations, chemists can exploit the structural features of $name$ to access enantiomerically pure compounds and optimize their pharmacological profiles.Overall, the strategic use of 1-(4-Aminophenyl)cyclopentanecarboxylic acid in chemical synthesis allows for the efficient construction of diverse organic compounds with therapeutic potential and structural diversity. Its role as a versatile building block highlights its importance in drug discovery and materials science, paving the way for the development of innovative pharmaceuticals and functional materials.