1. Home
  2. 3-Pyridinecarboxylic acid, 6-ethoxy-

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-Pyridinecarboxylic acid, 6-ethoxy-

CCOc1ccc(cn1)C(=O)O Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 6-ethoxy-
CAS Number: 97455-65-7
Product Number: AG00IJY7(AGN-PC-0LU6GB)
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

Request for Quotation

Customer Feedback

Chemical Structure


6-Ethoxynicotinic acid is a versatile chemical compound that finds widespread applications in the field of chemical synthesis. This compound is renowned for its ability to act as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. In particular, it is utilized as a crucial intermediate in the preparation of novel heterocyclic compounds with diverse biological activities.One of the primary applications of 6-Ethoxynicotinic acid is in the production of custom-designed drug molecules. By efficiently incorporating this compound into the synthesis pathway, chemists can achieve specific modifications to the molecular structure of potential therapeutic agents. This tailored approach enables the development of new drugs with enhanced efficacy, reduced side effects, and improved bioavailability.Moreover, 6-Ethoxynicotinic acid plays a pivotal role in the synthesis of agrochemicals that are essential for modern agricultural practices. By harnessing the unique reactivity of this compound, researchers can design innovative pesticides, herbicides, and fungicides with increased selectivity and reduced environmental impact. These improved agricultural products contribute significantly to crop protection and yield enhancement.Furthermore, in the realm of materials science, 6-Ethoxynicotinic acid serves as a valuable precursor for the preparation of functional materials with advanced properties. Through controlled chemical transformations, scientists can tailor the physical and chemical characteristics of these materials for diverse applications such as sensors, catalysts, and electronic devices. This versatility underscores the importance of 6-Ethoxynicotinic acid as a key ingredient in cutting-edge material synthesis strategies.In summary, the application of 6-Ethoxynicotinic acid in chemical synthesis is instrumental in the creation of novel pharmaceuticals, agrochemicals, and functional materials. Its role as a versatile building block enables the development of tailored compounds with targeted properties, fostering innovation and advancement in various industries.