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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-Pyridinecarboxylic acid, 5-amino-2-methoxy-, methyl ester

COC(=O)c1cc(N)cnc1OC Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 5-amino-2-methoxy-, methyl ester
CAS Number: 122433-51-6
Product Number: AG00177V(AGN-PC-0017HD)
Synonyms:
MDL No:
Molecular Formula: C8H10N2O3
Molecular Weight: 182.1766

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
182.179g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
182.069g/mol
Monoisotopic Mass:
182.069g/mol
Topological Polar Surface Area:
74.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
186
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 5-amino-2-methoxynicotinate is a versatile compound utilized in chemical synthesis for its unique properties. This compound serves as a key building block in the production of various pharmaceutical intermediates and fine chemicals. Its presence in chemical reactions enables the modification and functionalization of organic molecules, essential in the creation of complex structures for drug development and material science applications. With its strategic placement, Methyl 5-amino-2-methoxynicotinate plays a crucial role in the synthesis of diverse compounds with potential therapeutic or industrial significance.