249291-79-0

Basic information

• Product Name: 6-CHLORO-3-IODO-2-METHYLPYRIDINE
• Synonyms: Pyridine,6-chloro-3-iodo-2-methyl-;6-CHLORO-3-IODO-2-METHYLPYRIDINE;2-Chloro-5-iodo-6-methylpyridine
• CAS NO: 249291-79-0
• Molecular Formula: C₆H₅ClIN
• Molecular Weight: 253.46807
• Product Categories: Heterocyclic Compounds;Pyridines
• Mol File: 249291-79-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 30-33°C
• Boiling Point: 260.4 °C at 760 mmHg
• Flash Point: 111.3 °C
• Appearance: /
• Density: 1.906 g/cm³
• Vapor Pressure: 0.0199mmHg at 25°C
• Refractive Index: 1.624
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: -1.04±0.10(Predicted)
• Sensitive: Light Sensitive
• CAS DataBase Reference: 6-CHLORO-3-IODO-2-METHYLPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-CHLORO-3-IODO-2-METHYLPYRIDINE(249291-79-0)
• EPA Substance Registry System: 6-CHLORO-3-IODO-2-METHYLPYRIDINE(249291-79-0)

Safety Data

• PackingGroup: III
• Hazardous Substances Data: 249291-79-0(Hazardous Substances Data)

Usage

General Description

6-Chloro-3-iodo-2-methylpyridine is a chemical compound with the molecular formula C6H5ClIN. It is a pyridine derivative that contains chlorine, iodine, and a methyl group attached to the pyridine ring. 6-CHLORO-3-IODO-2-METHYLPYRIDINE is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used in organic synthesis as a building block for creating more complex molecules. 6-Chloro-3-iodo-2-methylpyridine may be used as a reagent in chemical reactions, and its properties and reactivity make it a valuable component in the field of synthetic chemistry.

InChI:InChI=1/C6H5ClIN/c1-4-5(8)2-3-6(7)9-4/h2-3H,1H3

Upstream product

• 132606-40-7 3-bromo-6-chloro-2-methyl-pyridine 
• 1575836-78-0 2-bromomethyl-6-chloro-3-iodopyridine 
• 1824-81-3 2-Amino-6-methylpyridine 
• 75073-11-9 5-iodo-6-methyl-pyridin-2-ylamine 

Downstream Products

• 1575831-00-3 1-(2'-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-7'H-spiro[azetidine-3,5'-furo[3,4-b]pyridine]-1-yl)-2-(methylsulfonyl)ethanone 
• 1575836-90-6 tert-butyl 2'-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-7'H-spiro[azetidine-3,5'-furo[3,4-b]pyridine]-1-carboxylate 
• 1575836-93-9 2'-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-7'H-spiro[azetidine-3,5'-furo[3,4-b]pyridine] trifluoroacetate 

Relevant articles and documents

Synthesis of conformationally constrained spirodihydrofuropyridine analogues of epibatidine

Conformationally constrained spirofuropyridine analogues of epibatidine, syn-2 and anti-2, in which the 7-azabicyclo[2.2.1]heptane system and the 2-chloropyridine ring are held rigidly with the shorter and longer N-N distances, respectively, were synthesized from N-Boc-7-azabicyclo[2.2.1]heptan-2-one. The preliminary binding studies suggested that syn-2 has stronger binding affinity for nAChRs than anti-2.

SPIROCYCLIC ISOXAZOLINES AS ANTIPARASITIC AGENTS

The invention recites spirocyclic isoxazoline derivatives of Formula (1) stereoisomers thereof, veterinary or pharmaceutical acceptable salts thereof, compositions thereof, processes for making, and their use as a parasiticide in an animal. The variables