CAS 28712-49-4
:Thiophene, 2-chloro-5-iodo-
Description:
Thiophene, 2-chloro-5-iodo- is a heterocyclic organic compound characterized by a five-membered aromatic ring containing sulfur. The presence of chlorine and iodine substituents at the 2 and 5 positions, respectively, influences its chemical reactivity and physical properties. This compound typically exhibits a pale yellow to brownish color and has a distinct aromatic odor. It is soluble in organic solvents such as dichloromethane and ether but has limited solubility in water due to its non-polar characteristics. The presence of halogens can enhance its reactivity, making it useful in various chemical syntheses, including the development of pharmaceuticals and agrochemicals. Additionally, thiophene derivatives are known for their applications in organic electronics, particularly in the fabrication of conductive polymers. Safety precautions should be taken when handling this compound, as halogenated compounds can pose health risks. Overall, thiophene, 2-chloro-5-iodo- is a valuable compound in organic chemistry with diverse applications.
Formula:C4H2ClIS
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Found 3 products.
Thiophene, 2-chloro-5-iodo-
CAS:Formula:C4H2ClISPurity:95%Color and Shape:LiquidMolecular weight:244.48122-chloro-5-iodothiophene
CAS:<p>2-Chloro-5-iodothiophene is a chlorinated aromatic compound that is used to produce various drugs and pesticides. This chemical is synthesized by the reaction of 2-chloro-5-iodobenzoic acid with phosphorus pentoxide or aluminium hydride in the presence of lithium aluminum hydride. 2-Chloro-5-iodothiophene has long lasting effects on behavior and can be used for the treatment of neuroleptic disorders. It was also shown to have antihistamine properties and may be used as an antipyretic drug. 2-Chloro-5-iodothiophene can inhibit the activity of acetylcholinesterase, which is responsible for breaking down acetylcholine, leading to paralysis and death by respiratory arrest.</p>Formula:C4H2ClISPurity:Min. 95%Molecular weight:244.47 g/mol


