CAS 28177-54-0

Phenol, 2,6-diiodo-

Description:

2,6-Diiodophenol is an organic compound characterized by the presence of two iodine atoms attached to the phenolic ring at the 2 and 6 positions. This compound is a derivative of phenol, which is known for its aromatic properties and hydroxyl functional group (-OH). The introduction of iodine atoms significantly influences its chemical behavior, enhancing its reactivity and potentially altering its solubility in various solvents. 2,6-Diiodophenol may exhibit antibacterial and antifungal properties, making it of interest in medicinal chemistry and materials science. It is typically a solid at room temperature and may appear as a crystalline or powdery substance. The presence of iodine also contributes to its color, often resulting in a darker hue compared to non-iodinated phenols. Safety precautions should be taken when handling this compound, as iodine can be hazardous. Overall, 2,6-diiodophenol serves as a valuable compound in various chemical applications, including synthesis and research.

Formula: C₆H₄I₂O

2,6-Diiodophenol

CAS: 28177-54-0

Formula: C₆H₄I₂O

Purity: 95%

Color and Shape: Solid

Molecular weight: 345.9043

Ref: IN-DA01BVSS

2,6-diiodophenol

CAS: 28177-54-0

2,6-diiodophenol

Purity: ≥95%

Molecular weight: 345.90g/mol

Ref: 54-OR97065

2,6-Diiodophenol

CAS: 28177-54-0

Color and Shape: Neat

Ref: 86-MM0694.18

2,6-Diiodophenol

CAS: 28177-54-0

Formula: C₆H₄I₂O

Molecular weight: 345.91

Ref: 4Z-T-4225

2,6-Diiodophenol

CAS: 28177-54-0

Purity: 95%

Molecular weight: 345.9060059

Ref: 10-F621803

2,6-Diiodophenol

Controlled Product

CAS: 28177-54-0

Applications 2,6-Diiodophenol is a useful reactant in organic synthesis.
References Gebara, Karimi S., et al.: Tetrahedron Let., 52(22), 2849-2852 (2011);Lv, Chunjie, et al.: Org. Let., 20(7), 1919-1923 (2018)

Formula: C₆H₄I₂O

Color and Shape: Neat

Molecular weight: 345.90

Ref: TR-D458920

2,6-Diiodophenol

CAS: 28177-54-0

2,6-Diiodophenol is a noncompetitive inhibitor that binds to the active site of carbonic anhydrase. It can be used as a pharmaceutical formulation or in sample preparation for gene sequence analysis. 2,6-Diiodophenol has been shown to have competitive inhibition against other inhibitors such as acetazolamide and dichlorphenamide. The marine sponge-derived enzyme carbonic anhydrase (CA) from the Gulf of Mexico was examined by chromatographic and spectroscopic methods. The CA activity was found to be inhibited by 2,6-diiodophenol in a concentration dependent manner with a KI value of 0.06 mM. 2,6-Diiodophenol also inhibits CA activity in rat liver microsomes at concentrations above 1 mM but does not inhibit peroxide production by the microsomal system at concentrations up to 10 mM. The crystal structure of 2,6-diiodophenol bound to CA has been determined using X

Formula: C₆H₄I₂O

Purity: Min. 95%

Molecular weight: 345.9 g/mol

Ref: 3D-DBA17754

2,6-Diiodophenol

CAS: 28177-54-0

Formula: C₆H₄I₂O

Molecular weight: 345.91

Ref: ST-EA-CP-L18066