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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-6-YL)PROPANOIC ACID

OC(=O)C(c1ccc2c(c1)cccn2)C Request for Quotation
Chemical Name: 2-(QUINOLIN-6-YL)PROPANOIC ACID
CAS Number: 959585-30-9
Product Number: AG00H672(AGN-PC-025PC4)
Synonyms:
MDL No:
Molecular Formula: C12H11NO2
Molecular Weight: 201.2212

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
201.225g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
201.079g/mol
Monoisotopic Mass:
201.079g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
242
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


2-(Quinolin-6-yl)propanoic acid is a versatile compound that finds wide application in chemical synthesis. It serves as a valuable building block for the construction of various organic molecules due to its unique structure and reactivity. This compound can be utilized in the synthesis of pharmaceutical intermediates, agrochemicals, and materials science. Its functional groups allow for facile derivatization, enabling the introduction of different substituents for diverse chemical transformations. In addition, the presence of the quinoline ring offers potential for further modification, leading to the development of new compounds with targeted properties. Therefore, 2-(Quinolin-6-yl)propanoic acid plays a crucial role in the synthesis of complex organic molecules with significant applications in various fields of chemistry.