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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)-

2-chloro-5-hydroxypyridine-4-carboxylic acid

Clc1ncc(c(c1)C(=O)O)O Request for Quotation
Chemical Name: 2-chloro-5-hydroxypyridine-4-carboxylic acid
CAS Number: 1060804-57-0
Product Number: AG003GZ0(AGN-PC-09R4JB)
Synonyms:
MDL No:
Molecular Formula: C6H4ClNO3
Molecular Weight: 173.5539

Identification/Properties

Properties
BP:
538.6±50.0°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
173.552g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
172.988g/mol
Monoisotopic Mass:
172.988g/mol
Topological Polar Surface Area:
70.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
164
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


2-Chloro-5-hydroxyisonicotinic acid, also known as CHINA, is a versatile and important compound in chemical synthesis. It serves as a key building block in the production of pharmaceuticals, agrochemicals, and functional materials due to its unique structural properties. In chemical synthesis, 2-Chloro-5-hydroxyisonicotinic acid is valued for its ability to undergo various reactions, including esterification, amidation, and nucleophilic substitution. These reactions enable the synthesis of complex molecules with specific functions and properties. The presence of both a chloro and hydroxy functional group in its structure provides opportunities for selective modifications, allowing chemists to tailor the compound for specific applications. 2-Chloro-5-hydroxyisonicotinic acid is particularly useful in the synthesis of biologically active compounds, such as antiviral drugs, anti-tumor agents, and herbicides, making it a valuable tool in medicinal and agricultural chemistry. Furthermore, its compatibility with a wide range of reaction conditions and its relatively low cost make 2-Chloro-5-hydroxyisonicotinic acid a popular choice for researchers and industry professionals alike seeking to synthesize novel compounds with high efficiency and efficacy.