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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)-

3-Quinolinecarboxylic acid, 4,6-dichloro-, ethyl ester

CCOC(=O)c1cnc2c(c1Cl)cc(cc2)Cl Request for Quotation
Chemical Name: 3-Quinolinecarboxylic acid, 4,6-dichloro-, ethyl ester
CAS Number: 21168-41-2
Product Number: AG007OWL(AGN-PC-0K5SO4)
Synonyms:
MDL No:
Molecular Formula: C12H9Cl2NO2
Molecular Weight: 270.1114

Identification/Properties

Computed Properties
Molecular Weight:
270.109g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
269.001g/mol
Monoisotopic Mass:
269.001g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
288
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Quinolinecarboxylic acid, 4,6-dichloro-, ethyl ester is a versatile chemical compound widely utilized in organic synthesis. It serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. With its unique structure and functional groups, this compound is crucial in the development of novel compounds with diverse biological activities.One notable application of 3-Quinolinecarboxylic acid, 4,6-dichloro-, ethyl ester is its use as a building block in the synthesis of quinoline-based drugs. By undergoing various chemical transformations, this compound can be modified to introduce different substituents and functional groups, leading to the development of analogs with enhanced pharmacological properties.Additionally, 3-Quinolinecarboxylic acid, 4,6-dichloro-, ethyl ester plays a pivotal role in the preparation of pesticides and herbicides. Its incorporation into the molecular structure of agrochemicals imparts desirable properties such as potency, selectivity, and stability, making it a valuable component in the agricultural industry.Furthermore, this compound can be employed in the synthesis of specialty chemicals and materials with specific industrial applications. Its chemical reactivity and compatibility with a wide range of functional groups make it a valuable tool for chemists and researchers seeking to develop innovative compounds for various purposes.