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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)-

1,8-Naphthyridine-3-carboxylic acid, 4-hydroxy-7-methyl-

Cc1ccc2c(n1)ncc(c2O)C(=O)O Request for Quotation
Chemical Name: 1,8-Naphthyridine-3-carboxylic acid, 4-hydroxy-7-methyl-
CAS Number: 13250-97-0
Product Number: AG0010RE(AGN-PC-0O125V)
Synonyms:
MDL No:
Molecular Formula: C10H8N2O3
Molecular Weight: 204.1821

Identification/Properties

Properties
MP:
278-280℃ (decomp)
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
204.185g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
204.053g/mol
Monoisotopic Mass:
204.053g/mol
Topological Polar Surface Area:
79.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
338
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-7-methyl-1,8-naphthyridine-3-carboxylic acid, a versatile chemical compound frequently employed in chemical synthesis, exhibits remarkable utility across a variety of applications. Its role as a key intermediate in the synthesis of pharmaceuticals and agrochemicals underscores its importance in the realm of organic chemistry. Through strategic manipulation of its functional groups, this compound serves as a crucial building block in the creation of novel molecules with diverse biological activities. Its precise structure and reactivity make it an indispensable tool for chemists seeking to develop innovative synthetic routes and functional materials. In particular, its involvement in the design and production of bioactive compounds highlights its significance in advancing research and development efforts within the scientific community.