1. Home
  2. 3-Pyridinecarboxylic acid, 2-chloro-4-fluoro-

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)-

3-Pyridinecarboxylic acid, 2-chloro-4-fluoro-

OC(=O)c1c(F)ccnc1Cl Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 2-chloro-4-fluoro-
CAS Number: 929022-76-4
Product Number: AG0036TX(AGN-PC-09RR76)
Synonyms:
MDL No:
Molecular Formula: C6H3ClFNO2
Molecular Weight: 175.5449

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
175.543g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
174.984g/mol
Monoisotopic Mass:
174.984g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
167
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Chloro-4-fluoronicotinic acid is a versatile chemical compound that finds wide application in chemical synthesis processes. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it an important intermediate in the production of diverse chemical compounds.One prominent application of 2-Chloro-4-fluoronicotinic acid lies in its utilization as a starting material for the synthesis of novel drug molecules. By incorporating this acid into the synthesis pathway, chemists can introduce specific functional groups or structural motifs that are crucial for the desired biological activity of the target drug. This acid's ability to participate in various chemical reactions, such as coupling reactions and substitution reactions, enables chemists to create complex molecular structures efficiently.Furthermore, 2-Chloro-4-fluoronicotinic acid plays a significant role in the development of agrochemicals. By using this compound as a precursor, chemists can design and synthesize potent pesticides, herbicides, and fungicides with enhanced efficacy and selectivity. The presence of the chlorine and fluorine atoms in the acid's structure allows for the introduction of substituents that can impart desired properties to the final agrochemical product.In the realm of specialty chemicals, 2-Chloro-4-fluoronicotinic acid serves as a valuable building block for the synthesis of fine chemicals, dyestuffs, and materials with specific applications. Its versatility and reactivity make it a preferred choice for chemists engaged in the development of innovative chemical products.In conclusion, the application of 2-Chloro-4-fluoronicotinic acid in chemical synthesis is multifaceted and crucial for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its strategic use as a key intermediate allows chemists to access a diverse array of complex molecules with tailored properties and functionalities essential for modern chemical industries.