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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)-

6-Hydroxy-5-methoxynicotinic acid

COc1cc(c[nH]c1=O)C(=O)O Request for Quotation
Chemical Name: 6-Hydroxy-5-methoxynicotinic acid
CAS Number: 1171919-98-4
Product Number: AG000DVY(AGN-PC-0WAH0T)
Synonyms:
MDL No:
Molecular Formula: C7H7NO4
Molecular Weight: 169.1348

Identification/Properties

Computed Properties
Molecular Weight:
169.136g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
169.038g/mol
Monoisotopic Mass:
169.038g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
290
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


6-Hydroxy-5-methoxynicotinic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and complex organic molecules. With its unique structural properties, $name$ plays a vital role in the development of innovative drugs and chemical processes. In chemical synthesis, it acts as a key intermediate, facilitating the formation of diverse molecular structures and enabling the synthesis of novel compounds with valuable biological activities. As a result, 6-Hydroxy-5-methoxynicotinic acid is a valuable tool for chemists working in the fields of medicinal chemistry, agricultural chemistry, and organic synthesis.