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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, 6-(phenylmethoxy)-

OC(=O)c1ccc(nc1)OCc1ccccc1 Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 6-(phenylmethoxy)-
CAS Number: 94084-76-1
Product Number: AG00GSH3(AGN-PC-0JP2VS)
Synonyms:
MDL No:
Molecular Formula: C13H11NO3
Molecular Weight: 229.2313

Identification/Properties

Computed Properties
Molecular Weight:
229.235g/mol
XLogP3:
2.2
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:
251
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-(Benzyloxy)nicotinic acid, also known as Benzonicoic acid, is a versatile compound commonly utilized in chemical synthesis processes. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and organic intermediates. Due to its unique structure and reactivity, 6-(Benzyloxy)nicotinic acid enables the introduction of the nicotinic acid moiety into diverse molecular frameworks, allowing for the creation of novel compounds with potential biological activities. In organic synthesis, this compound can undergo various transformations such as esterification, amidation, and Suzuki-Miyaura coupling reactions to generate structurally complex molecules of interest. Additionally, 6-(Benzyloxy)nicotinic acid is frequently employed as a protecting group strategy in multi-step synthesis routes to facilitate selective transformations and enhance overall synthetic efficiency. The diverse applications of 6-(Benzyloxy)nicotinic acid make it a valuable tool for chemists seeking to access a wide range of functionalized compounds with potential therapeutic or industrial significance.