1. Home
  2. 3-Pyridinol, 6-fluoro-2-iodo-

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-Pyridinol, 6-fluoro-2-iodo-

Fc1ccc(c(n1)I)O Request for Quotation
Chemical Name: 3-Pyridinol, 6-fluoro-2-iodo-
CAS Number: 214911-10-1
Product Number: AG0037KY(AGN-PC-02GQ11)
Synonyms:
MDL No:
Molecular Formula: C5H3FINO
Molecular Weight: 238.9863

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
238.988g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
238.924g/mol
Monoisotopic Mass:
238.924g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
103
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


6-Fluoro-3-hydroxy-2-iodopyridine is a versatile chemical compound that finds wide applications in organic chemistry, particularly in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural features and reactivity.In chemical synthesis, 6-Fluoro-3-hydroxy-2-iodopyridine can be utilized as a key intermediate in the preparation of biologically active compounds. Its functional groups allow for selective modifications and functionalization, enabling the introduction of specific substituents or structural motifs that are crucial for the desired biological activity.Furthermore, the presence of both fluorine and iodine atoms in the molecule imparts valuable properties to the final products, such as improved metabolic stability, enhanced binding affinity, or altered physicochemical properties. This makes 6-Fluoro-3-hydroxy-2-iodopyridine a valuable tool in medicinal chemistry, where small structural modifications can significantly impact the efficacy and safety of drugs.Overall, the strategic incorporation of 6-Fluoro-3-hydroxy-2-iodopyridine in chemical synthesis allows researchers to access a diverse array of functionalized compounds with potential applications in drug discovery, material science, and other fields requiring complex molecular design.