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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)-

2-quinolin-2-ylacetic acid;hydrochloride

OC(=O)Cc1ccc2c(n1)cccc2.Cl Request for Quotation
Chemical Name: 2-quinolin-2-ylacetic acid;hydrochloride
CAS Number: 25888-68-0
Product Number: AG006V7M(AGN-PC-0NK9LU)
Synonyms:
MDL No:
Molecular Formula: C11H10ClNO2
Molecular Weight: 223.6556

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;

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


2-(Quinolin-2-yl)acetic acid hydrochloride is a versatile compound widely utilized in chemical synthesis, particularly in the pharmaceutical and fine chemical industries. Its unique chemical structure allows for diverse applications in the creation of various organic compounds.One prominent use of 2-(Quinolin-2-yl)acetic acid hydrochloride is as a key building block in the synthesis of heterocyclic compounds. By reacting this compound with other suitable reagents, chemists can access a wide array of structurally complex molecules that are crucial for drug discovery and development. Its ability to serve as a precursor in the construction of biologically active molecules makes it an invaluable tool in medicinal chemistry research.Furthermore, 2-(Quinolin-2-yl)acetic acid hydrochloride can also be employed in the synthesis of fluorescent dyes and imaging agents due to its aromatic properties and potential for conjugation with other fluorophores. These fluorescent derivatives find applications in various biological assays, imaging studies, and diagnostic tools, making them essential in the field of chemical biology.Overall, the utilization of 2-(Quinolin-2-yl)acetic acid hydrochloride in chemical synthesis showcases its significance as a key intermediate in the creation of diverse compounds with significant implications in various industries, particularly in drug discovery and biological research.