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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)-

2-Pyridinecarboxylic acid, 5-ethoxy-

CCOc1ccc(nc1)C(=O)O Request for Quotation
Chemical Name: 2-Pyridinecarboxylic acid, 5-ethoxy-
CAS Number: 98353-08-3
Product Number: AG00IK2O(AGN-PC-03ZRBT)
Synonyms:
MDL No:
Molecular Formula: C8H9NO3
Molecular Weight: 167.1620

Identification/Properties

Computed Properties
Molecular Weight:
167.164g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
167.058g/mol
Monoisotopic Mass:
167.058g/mol
Topological Polar Surface Area:
59.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
160
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Ethoxypicolinic acid is a versatile compound that has found numerous applications in chemical synthesis. As a specialized organic building block, it serves as a key component in the creation of various pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity make it particularly valuable in the development of new molecules with targeted properties.In chemical synthesis, 5-Ethoxypicolinic acid can be utilized as a starting material for the construction of more complex molecules through various transformation reactions. Its ethoxy and picolinic acid functional groups offer convenient sites for derivatization, allowing for the introduction of different substituents or modifications to tailor the properties of the final product. Additionally, its compatibility with a wide range of coupling reactions enables efficient bond formation with other molecules to generate structurally diverse compounds.Moreover, 5-Ethoxypicolinic acid's ability to act as a chelating agent for metal ions further expands its utility in catalysis and coordination chemistry. By coordinating with metal centers, it can facilitate specific reactions or enhance the selectivity of catalytic processes, leading to improved efficiency and control in synthetic transformations.Overall, the versatile nature of 5-Ethoxypicolinic acid makes it a valuable tool in chemical synthesis, offering opportunities for the development of novel compounds with distinct properties and applications.