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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)-

5-(3,5-dimethylphenyl)pyridine-3-carboxylic acid

Cc1cc(C)cc(c1)c1cncc(c1)C(=O)O Request for Quotation
Chemical Name: 5-(3,5-dimethylphenyl)pyridine-3-carboxylic acid
CAS Number: 1048486-24-3
Product Number: AG00941Y(AGN-PC-07XW8Q)
Synonyms:
MDL No:
Molecular Formula: C14H13NO2
Molecular Weight: 227.2585

Identification/Properties

Computed Properties
Molecular Weight:
227.263g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
227.095g/mol
Monoisotopic Mass:
227.095g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
269
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


5-(3,5-Dimethylphenyl)nicotinic acid is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. This compound is often employed as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its functional groups allow for facile modification and transformation, making it an essential building block for a range of organic reactions.In chemical synthesis, 5-(3,5-Dimethylphenyl)nicotinic acid serves as a valuable substrate for the preparation of biologically active compounds, such as anti-inflammatory agents, antiviral drugs, and enzyme inhibitors. Its aromatic ring system and carboxylic acid functionality enable derivatization through various synthetic routes, including esterification, amidation, and cross-coupling reactions.Furthermore, the presence of a nicotinic acid moiety in this compound imparts unique pharmacological properties, making it a promising candidate for drug discovery and development. Its structural features offer opportunities for enhancing the bioactivity, solubility, and pharmacokinetic profiles of potential drug candidates.Overall, the application of 5-(3,5-Dimethylphenyl)nicotinic acid in chemical synthesis underscores its significance as a versatile and valuable intermediate with broad utility in the pharmaceutical and agrochemical industries.