CAS 205444-22-0

2-chloro-4-iodo-6-(trifluoromethyl)pyridine

Description:

2-Chloro-4-iodo-6-(trifluoromethyl)pyridine is a heterocyclic aromatic compound characterized by its pyridine ring, which is a six-membered ring containing one nitrogen atom. This compound features a chlorine atom at the 2-position, an iodine atom at the 4-position, and a trifluoromethyl group (-CF3) at the 6-position of the pyridine ring. The presence of these substituents significantly influences its chemical properties, including its reactivity and polarity. The trifluoromethyl group is known for imparting strong electron-withdrawing characteristics, which can enhance the compound's electrophilicity. Additionally, the halogen substituents (chlorine and iodine) can participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. This compound is of interest in medicinal chemistry and materials science due to its potential applications in drug development and as a building block for more complex molecules. Its unique combination of halogen atoms and a trifluoromethyl group makes it a valuable compound for further research and synthesis in various chemical contexts.

Formula: C₆H₂ClF₃IN

InChI: InChI=1/C6H2ClF3IN/c7-5-2-3(11)1-4(12-5)6(8,9)10/h1-2H

SMILES: c1c(cc(Cl)nc1C(F)(F)F)I

Synonyms:

• Pyridine, 2-Chloro-4-Iodo-6-(Trifluoromethyl)-
• 2-Chloro-4-iodo-6-(trifluoromethyl)pyridine

Pyridine, 2-chloro-4-iodo-6-(trifluoromethyl)-

CAS: 205444-22-0

Formula: C₆H₂ClF₃IN

Purity: 98%

Color and Shape: Solid

Molecular weight: 307.4395

Ref: IN-DA002A35

2-Chloro-4-iodo-6-(trifluoromethyl)pyridine

CAS: 205444-22-0

2-Chloro-4-iodo-6-(trifluoromethyl)pyridine

Purity: 98%

Color and Shape: Light Tan Solid

Molecular weight: 307.44g/mol

Ref: 54-PC48602

2-Chloro-4-iodo-6-(trifluoromethyl)pyridine

CAS: 205444-22-0

Formula: C₆H₂ClF₃IN

Purity: 97%

Color and Shape: Solid

Molecular weight: 307.44

Ref: 10-F067318

2-Chloro-4-iodo-6-(trifluoromethyl)pyridine

CAS: 205444-22-0

2-Chloro-4,6-difluoro-pyridine is an electrophilic compound that can react with nucleophiles to form covalent bonds. This reaction is known as nucleophilic substitution and it can be used in the synthesis of organic compounds. The diisopropylamide of lithium is a popular reagent for this purpose because it is inexpensive, highly reactive, and easily purified by distillation. In particular, 2-chloro-4,6-difluoro-pyridine reacts quantitatively with lithium diisopropylamide to form 4-(2-chloro-4,6-difluoro)pyrimidin-2(1H)-ones in tetrahydrofuran.

Formula: C₆H₂ClF₃IN

Purity: Min. 95%

Color and Shape: Solid.

Molecular weight: 307.44 g/mol

Ref: 3D-FC87888