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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-(3-bromoquinolin-6-yl)acetic acid

OC(=O)Cc1ccc2c(c1)cc(cn2)Br Request for Quotation
Chemical Name: 2-(3-bromoquinolin-6-yl)acetic acid
CAS Number: 1022091-93-5
Product Number: AG0006X4(AGN-PC-0CUK80)
Synonyms:
MDL No:
Molecular Formula: C11H8BrNO2
Molecular Weight: 266.0907

Identification/Properties

Computed Properties
Molecular Weight:
266.094g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
264.974g/mol
Monoisotopic Mass:
264.974g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
247
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(3-Bromoquinolin-6-yl)acetic acid is a versatile compound widely used in chemical synthesis as a key building block for the creation of various organic molecules. This unique acid derivative plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials science due to its functional group reactivity and structural properties. Its incorporation in synthetic routes enables the efficient formation of complex molecular structures and facilitates the modification of specific regions within a molecule, leading to the synthesis of novel compounds with tailored properties. Additionally, the presence of the bromoquinoline moiety enhances the compound's potential for applications in medicinal chemistry, molecular probes, and material design, making it a valuable tool for researchers and chemists working in diverse fields of chemical science.