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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-aminoquinolin-2-yl) ethyl carbonate

CCOC(=O)Oc1nc2ccccc2cc1N Request for Quotation
Chemical Name: (3-aminoquinolin-2-yl) ethyl carbonate
CAS Number: 62235-59-0
Product Number: AG00EIFW(AGN-PC-0J0YD5)
Synonyms:
MDL No:
Molecular Formula: C12H12N2O3
Molecular Weight: 232.2353

Identification/Properties

Properties
MP:
148-150°C
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
216.24g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
216.09g/mol
Monoisotopic Mass:
216.09g/mol
Topological Polar Surface Area:
65.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
257
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 3-aminoquinoline-2-carboxylate, often abbreviated as EAQC, is a versatile compound widely used in chemical synthesis. Due to its unique structure, EAQC serves as a key building block in the creation of various pharmaceutical intermediates and bioactive molecules.In chemical synthesis, Ethyl 3-aminoquinoline-2-carboxylate plays a crucial role as a precursor in the preparation of diverse compounds with therapeutic potential. It can be utilized in the development of novel drugs, especially in the field of antimalarial and antitumor agents. Additionally, EAQC is valuable in the synthesis of heterocyclic compounds and complex organic molecules, offering opportunities for researchers to explore new chemical reactions and pathways.Moreover, Ethyl 3-aminoquinoline-2-carboxylate demonstrates excellent reactivity and compatibility with a wide range of functional groups, making it a preferred choice for various synthetic transformations. Its strategic incorporation into synthetic pathways allows chemists to efficiently access target molecules with high purity and yield.Overall, the application of Ethyl 3-aminoquinoline-2-carboxylate in chemical synthesis showcases its significant contribution to the advancement of medicinal chemistry and organic synthesis, enabling the development of innovative pharmaceuticals and biologically active compounds.