1. Home
  2. 3-Quinolinecarboxylic acid, 2-methyl-, ethyl ester

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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, 2-methyl-, ethyl ester

CCOC(=O)c1cc2ccccc2nc1C Request for Quotation
Chemical Name: 3-Quinolinecarboxylic acid, 2-methyl-, ethyl ester
CAS Number: 15785-08-7
Product Number: AG001PRG(AGN-PC-0JUB0Q)
Synonyms:
MDL No:
Molecular Formula: C13H13NO2
Molecular Weight: 215.2478

Identification/Properties

Properties
MP:
69-70℃
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
215.252g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
215.095g/mol
Monoisotopic Mass:
215.095g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
254
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#:
-
Hazard Statements:
H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Ethyl 2-methylquinoline-3-carboxylate is a versatile compound that finds wide application in chemical synthesis processes. As a key intermediate, it plays a crucial role in the production of various pharmaceuticals, agrochemicals, and functional materials.In organic synthesis, Ethyl 2-methylquinoline-3-carboxylate serves as a valuable building block for the construction of complex molecules. Its unique structural features make it a valuable precursor for the synthesis of heterocyclic compounds with diverse biological activities. This compound can be efficiently functionalized to introduce different substituent groups, allowing for the customization of the final product properties.One of the prominent applications of Ethyl 2-methylquinoline-3-carboxylate is in the preparation of novel drug candidates. By incorporating this intermediate into the synthesis route, chemists can access a range of potential pharmaceutical agents with enhanced pharmacological profiles. Furthermore, its use in the synthesis of agrochemicals enables the development of new compounds for crop protection and pest control.Overall, Ethyl 2-methylquinoline-3-carboxylate is a valuable tool in the arsenal of synthetic chemists, facilitating the creation of diverse compounds with important applications in the fields of medicine, agriculture, and materials science.