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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)-

Benzeneacetic acid, 3-(3-pyridinyl)-

OC(=O)Cc1cccc(c1)c1cccnc1 Request for Quotation
Chemical Name: Benzeneacetic acid, 3-(3-pyridinyl)-
CAS Number: 597584-62-8
Product Number: AG00EAP8(AGN-PC-0KKO07)
Synonyms:
MDL No:
Molecular Formula: C13H11NO2
Molecular Weight: 213.2319

Identification/Properties

Computed Properties
Molecular Weight:
213.236g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
213.079g/mol
Monoisotopic Mass:
213.079g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
242
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


2-(3-(Pyridin-3-yl)phenyl)acetic acid is a versatile compound that finds wide applications in chemical synthesis. This compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and materials due to its unique structure and reactivity. In organic synthesis, it acts as a valuable intermediate in the formation of heterocyclic compounds and complex organic molecules. Additionally, its ability to undergo different types of reactions, such as esterification, amidation, and cross-coupling, makes it a valuable tool in the creation of structurally diverse compounds. The presence of both a pyridine ring and a phenyl group in its structure enhances its chemical properties and allows for tuning of its reactivity in specific synthetic routes.