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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)-

4-Pyridinecarboxylic acid, 2-amino-, ethyl ester

CCOC(=O)c1ccnc(c1)N Request for Quotation
Chemical Name: 4-Pyridinecarboxylic acid, 2-amino-, ethyl ester
CAS Number: 13362-30-6
Product Number: AG003GJI(AGN-PC-0LW6P3)
Synonyms:
MDL No: MFCD03791260
Molecular Formula: C8H10N2O2
Molecular Weight: 166.1772

Identification/Properties

Properties
MP:
123.5-123.6°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
166.18g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
166.074g/mol
Monoisotopic Mass:
166.074g/mol
Topological Polar Surface Area:
65.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
161
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 2-aminoisonicotinate is a versatile compound commonly used in chemical synthesis as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique chemical structure allows for the introduction of the amino group into organic molecules, making it valuable in the development of bioactive compounds and pharmaceutical intermediates. In particular, Ethyl 2-aminoisonicotinate is often employed in the synthesis of drugs targeting neurological disorders, cancer treatments, and antimicrobial agents. Its compatibility with a wide range of reaction conditions and its ability to undergo functional group transformations make it a valuable tool for organic chemists seeking to access diverse molecular frameworks with enhanced biological activity.