1. Home
  2. Pentanoic acid, 4-[(6-methoxy-8-quinolinyl)amino]-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Pentanoic acid, 4-[(6-methoxy-8-quinolinyl)amino]-

COc1cc(NC(CCC(=O)O)C)c2c(c1)cccn2 Request for Quotation
Chemical Name: Pentanoic acid, 4-[(6-methoxy-8-quinolinyl)amino]-
CAS Number: 77229-68-6
Product Number: AG005OMZ(AGN-PC-088NJ1)
Synonyms:
MDL No:
Molecular Formula: C15H18N2O3
Molecular Weight: 274.3150

Identification/Properties

Properties
MP:
148-151°C
BP:
517.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-((6-Methoxyquinolin-8-yl)amino)pentanoic acid is a versatile compound that finds extensive application in chemical synthesis processes. This compound serves as a valuable building block for the creation of novel pharmaceuticals, agrochemicals, and materials with unique properties. Its structural characteristics make it an ideal precursor for the synthesis of various biologically active molecules and functionalized organic compounds.Specifically, in chemical synthesis, 4-((6-Methoxyquinolin-8-yl)amino)pentanoic acid can be utilized as a key intermediate in the preparation of drug candidates targeting specific biological pathways. By incorporating this compound into synthetic routes, chemists can access a diverse range of derivatives with tailored activities and improved pharmacokinetic profiles. Additionally, the presence of the quinoline moiety in its structure imparts desirable properties for biological interactions, making it a valuable component in medicinal chemistry endeavors.Moreover, the amino and carboxylic acid functional groups present in 4-((6-Methoxyquinolin-8-yl)amino)pentanoic acid offer multiple points for further derivatization and modifications, enabling the synthesis of new chemical entities with enhanced properties. Through strategic transformations and chemical manipulations, researchers can explore the full potential of this compound in the development of innovative molecules for various applications in the fields of medicine, agriculture, and materials science.