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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, 1,2,3,4-tetrahydro-2-oxo-, methyl ester

COC(=O)C1Cc2ccccc2NC1=O Request for Quotation
Chemical Name: 3-Quinolinecarboxylic acid, 1,2,3,4-tetrahydro-2-oxo-, methyl ester
CAS Number: 105404-33-9
Product Number: AG0095RQ(AGN-PC-01UHBX)
Synonyms:
MDL No:
Molecular Formula: C11H11NO3
Molecular Weight: 205.2099

Identification/Properties

Computed Properties
Molecular Weight:
205.213g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
205.074g/mol
Monoisotopic Mass:
205.074g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
277
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-Oxo-1,2,3,4-tetrahydroquinoline-3-carboxylic acid methyl ester functions as a key intermediate in chemical synthesis, particularly in the production of pharmaceuticals and agrochemicals. This compound plays a vital role in the creation of various medicinal products due to its unique structural properties and reactivity. Its functionality as a building block enables the synthesis of diverse compounds with therapeutic or agricultural applications. In pharmaceutical synthesis, this ester serves as a crucial component in the construction of bioactive molecules, allowing for the development of new drugs or modifications of existing ones. Similarly, in agrochemical synthesis, its incorporation facilitates the production of crop protection agents or pesticides with enhanced efficacy. Its versatility and utility make 2-Oxo-1,2,3,4-tetrahydroquinoline-3-carboxylic acid methyl ester a valuable asset in the realm of chemical synthesis.