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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-(pyridin-3-ylmethoxy)benzoic acid

OC(=O)c1cccc(c1)OCc1cccnc1 Request for Quotation
Chemical Name: 3-(pyridin-3-ylmethoxy)benzoic acid
CAS Number: 945473-82-5
Product Number: AG019V3B(AGN-PC-0161NX)
Synonyms:
MDL No:
Molecular Formula: C13H11NO3
Molecular Weight: 229.2313

Identification/Properties

Computed Properties
Molecular Weight:
229.235g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
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:
257
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


3-(Pyridin-3-ylmethoxy)benzoic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis. It serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. In particular, $name$ is frequently employed as a key intermediate in the synthesis of novel drug candidates due to its unique structure and reactivity. By acting as a functional group modifier, $name$ facilitates the introduction of specific chemical functionalities into target molecules, enabling the design and development of tailor-made compounds with enhanced bioactivity and properties. Additionally, the presence of the pyridine moiety in $name$ imparts pharmacological significance to the final products, making it an indispensable component in medicinal chemistry research and drug discovery endeavors. The strategic incorporation of 3-(Pyridin-3-ylmethoxy)benzoic acid in synthetic pathways enables chemists to access diverse libraries of compounds with valuable biological activities and potential therapeutic benefits.