Benzoic acid, 4-(6-methoxy-3-pyridinyl)-


Chemical Name: Benzoic acid, 4-(6-methoxy-3-pyridinyl)-
CAS Number: 219671-80-4
Product Number: AG006YDI(AGN-PC-0LF8SW)
Synonyms:
MDL No:
Molecular Formula: C13H11NO3
Molecular Weight: 229.2313

Identification/Properties


Computed Properties
Molecular Weight:
229.235g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
229.074g/mol
Monoisotopic Mass:
229.074g/mol
Topological Polar Surface Area:
59.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
261
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



The compound 4-(6-Methoxypyridin-3-yl)benzoic acid, often referred to as $name$, serves as a versatile building block in chemical synthesis. Its unique structure combines a pyridine ring with a benzene ring, offering a range of synthetic possibilities in various industries. In chemical synthesis, $name$ can be utilized in the production of pharmaceuticals, agrochemicals, and materials science. Its functional groups provide avenues for derivatization, allowing for the creation of new compounds with potentially enhanced properties. Additionally, the presence of the methoxy group on the pyridine ring can influence reactivity and selectivity in chemical reactions.Furthermore, $name$ can serve as a key intermediate in the preparation of advanced organic molecules, enabling the synthesis of complex structures with specific biological or physical properties. Its incorporation into molecular frameworks can lead to the development of novel drug candidates, crop protection agents, or materials with tailored functionalities.Overall, the strategic positioning of functional groups in 4-(6-Methoxypyridin-3-yl)benzoic acid makes it a valuable tool for chemists engaged in the design and synthesis of innovative compounds across various scientific disciplines.