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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, 4-hydroxy-2,6-dimethyl-

Cc1cc(O)c(c(n1)C)C(=O)O Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 4-hydroxy-2,6-dimethyl-
CAS Number: 33259-21-1
Product Number: AG00CLXY(AGN-PC-0O90DZ)
Synonyms:
MDL No:
Molecular Formula: C8H9NO3
Molecular Weight: 167.1620

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
167.164g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
167.058g/mol
Monoisotopic Mass:
167.058g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
312
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


4-Hydroxy-2,6-dimethylnicotinic acid, also known as HMNA, is a versatile compound widely used in chemical synthesis as a building block in the production of various pharmaceuticals, agrochemicals, and organic materials. This compound serves as a valuable intermediate in the synthesis of biologically active molecules due to its unique structural characteristics and reactivity.In chemical synthesis, 4-Hydroxy-2,6-dimethylnicotinic acid plays a crucial role as a key starting material for the preparation of diverse derivatives with enhanced properties. Its hydroxy and methyl substituents provide strategic functional groups that can be easily modified to introduce specific chemical functionalities. These modifications can be tailored to achieve desired molecular structures and properties, making it an essential component in the development of novel compounds for various applications.Furthermore, the presence of a hydroxy group in 4-Hydroxy-2,6-dimethylnicotinic acid offers opportunities for selective derivatization and subsequent transformations, enabling the synthesis of complex molecules with high efficiency and precision. With its broad utility in chemical synthesis, this compound serves as a valuable platform for designing and synthesizing a wide range of advanced materials and bioactive substances with potential industrial and pharmaceutical applications.