CAS 2401-25-4
:1-Chloro-2-iodo-4-methoxybenzene
Description:
1-Chloro-2-iodo-4-methoxybenzene, also known by its CAS number 2401-25-4, is an organic compound that belongs to the class of halogenated aromatic compounds. It features a benzene ring substituted with three distinct groups: a chlorine atom, an iodine atom, and a methoxy group (-OCH3). The presence of these halogen substituents significantly influences its chemical reactivity and physical properties. Typically, this compound appears as a colorless to pale yellow liquid or solid, depending on the temperature and purity. It is generally insoluble in water but soluble in organic solvents such as ethanol and ether. The methoxy group contributes to its electron-donating properties, which can affect the compound's reactivity in electrophilic aromatic substitution reactions. Additionally, the halogen atoms can participate in nucleophilic substitution reactions, making this compound useful in various synthetic applications in organic chemistry. Safety precautions should be taken when handling this compound, as both chlorine and iodine are hazardous substances.
Formula:C7H6ClIO
InChI:InChI=1S/C7H6ClIO/c1-10-5-2-3-6(8)7(9)4-5/h2-4H,1H3
InChI key:InChIKey=CKEGHWVVAIEDPU-UHFFFAOYSA-N
SMILES:O(C)C1=CC(I)=C(Cl)C=C1
Synonyms:- 4-Chloro-3-iodoanisole
- 4-Chloro-3-iodophenyl methyl ether
- Anisole, 4-chloro-3-iodo-
- Benzene, 1-chloro-2-iodo-4-methoxy-
- 1-Chloro-2-iodo-4-methoxybenzene
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Found 4 products.
4-Chloro-3-iodoanisole
CAS:<p>4-Chloro-3-iodoanisole is a tetracyclic organic compound. It is an intermediate in the synthesis of arynes and dienes by dehalogenation of substituted benzenes with organolithium reagents. 4CI has been shown to react with dienophiles, such as 1,2-dichlorobenzene, to give the corresponding ethylenic products. The yield of this reaction is dependent on steric factors, such as the electronic nature of substituents on the benzene ring and their orientation relative to one another.</p>Formula:C7H6ClIOPurity:Min. 95%Molecular weight:268.48 g/mol
