1. Home
  2. 2-Pyridinecarboxylic acid, 3-chloro-5-nitro-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-Pyridinecarboxylic acid, 3-chloro-5-nitro-

[O-][N+](=O)c1cnc(c(c1)Cl)C(=O)O Request for Quotation
Chemical Name: 2-Pyridinecarboxylic acid, 3-chloro-5-nitro-
CAS Number: 141238-23-5
Product Number: AG001G3V(AGN-PC-025BYZ)
Synonyms:
MDL No:
Molecular Formula: C6H3ClN2O4
Molecular Weight: 202.5520

Identification/Properties

Computed Properties
Molecular Weight:
202.55g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
201.978g/mol
Monoisotopic Mass:
201.978g/mol
Topological Polar Surface Area:
96A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
229
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

Request for Quotation

Customer Feedback

Chemical Structure


3-Chloro-5-nitropicolinic acid, also known as $name$, serves as a valuable reagent in chemical synthesis due to its unique chemical properties. This compound is commonly utilized in organic chemistry reactions as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its versatile nature allows it to participate in a wide range of transformations, making it a powerful tool for medicinal and materials chemistry research. In particular, 3-Chloro-5-nitropicolinic acid can function as a precursor in the formation of heterocyclic compounds, which are essential structural motifs found in many biologically active molecules. By incorporating this compound into synthetic pathways, chemists can access novel compounds with enhanced biological activities or tailored physical properties for specific applications. Additionally, the functional groups present in 3-Chloro-5-nitropicolinic acid enable researchers to introduce further modifications, such as derivatization or cross-coupling reactions, to fine-tune the properties of the final product. The strategic incorporation of 3-Chloro-5-nitropicolinic acid in chemical synthesis plays a crucial role in expanding the synthetic toolbox available to chemists and advancing the discovery of new molecules with potential therapeutic or industrial relevance.