CAS 202982-72-7

4-Chloro-3-iodophenol

Description:

4-Chloro-3-iodophenol is an organic compound characterized by the presence of both chlorine and iodine substituents on a phenolic ring. It features a hydroxyl group (-OH) attached to a benzene ring, which is further substituted at the 3 and 4 positions with iodine and chlorine atoms, respectively. This compound typically appears as a solid and is known for its potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of halogens can influence its reactivity, making it a useful intermediate in organic synthesis. Additionally, 4-Chloro-3-iodophenol may exhibit antimicrobial properties, which can be beneficial in developing antiseptic agents. Its solubility in organic solvents and limited solubility in water are typical for halogenated phenols, affecting its behavior in different chemical environments. Safety precautions should be taken when handling this compound, as halogenated phenols can be toxic and may pose environmental hazards. Overall, 4-Chloro-3-iodophenol is a significant compound in chemical research and industrial applications.

Formula: C₆H₄ClIO

InChI: InChI=1/C6H4ClIO/c7-5-2-1-4(9)3-6(5)8/h1-3,9H

InChI key: InChIKey=UPIATGHEVZKVRT-UHFFFAOYSA-N

SMILES: IC1=C(Cl)C=CC(O)=C1

Synonyms:

• Phenol, 4-Chloro-3-Iodo-
• 4-Chloro-3-iodophenol
• 4-Chloro-1-hydroxy-3-iodobenzene

Phenol, 4-chloro-3-iodo-

CAS: 202982-72-7

Formula: C₆H₄ClIO

Purity: 98%

Color and Shape: Solid

Molecular weight: 254.4528

Ref: IN-DA0028LL

4-Chloro-3-iodophenol, min. 98%

CAS: 202982-72-7

Formula: C₆H₄ClIO

Purity: min. 98%

Color and Shape: White solid

Molecular weight: 254.45

Ref: 08-06-0083

4-Chloro-3-iodophenol

CAS: 202982-72-7

4-Chloro-3-iodophenol

Formula: C₆H₄ClIO

Purity: ≥95%

Color and Shape: white solid

Molecular weight: 254.45g/mol

Ref: 54-OR2164

4-Chloro-3-iodophenol

CAS: 202982-72-7

4-Chloro-3-iodophenol is a reactive chemical substance that can be used as a reagent in the synthesis of diagnostic agents, sunscreens and disinfectants. The reaction rate is increased by the presence of chlorine and other halogens such as iodine or bromine. 4-Chloro-3-iodophenol reacts with triclosan to form chlorinated trihalomethanes, which are more efficient disinfectants than their nonchlorinated counterparts. However, 4-chloro-3-iodophenol can also react with the oxidant hydrogen peroxide to form an unstable intermediate compound that degrades into toxic products like hypochlorous acid and chloramines. This instability makes this substance unsuitable for use in certain applications such as water purification.

Formula: C₆H₄ClIO

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 254.45 g/mol

Ref: 3D-FC70239

4-Chloro-3-iodophenol

CAS: 202982-72-7

Formula: C₆H₄ClIO

Purity: 95%

Color and Shape: Liquid, No data available.

Molecular weight: 254.45

Ref: 10-F231335