The presence of two iodine atoms significantly increases molecular weight and polarizability, while the phenolic –OH group provides a reactive hydrogen-bond donor site. This compound features a benzofuran core substituted with a butyl chain at the 2-position, enhancing hydrophobic character, and a 4-hydroxy-3,5-diiodophenyl moiety connected through a ketone (carbonyl) linkage.
(2-Butylbenzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) ketone
| API Name | Amiodarone |
|---|---|
| CAS No | 1951-26-4 |
| Molecular Formula | C19H16I2O3 |
| Molecular Weight | 546.1 g/mol |
| Synonyms | (2-butyl-1-benzofuran-3-yl)-(4-hydroxy-3,5-diiodophenyl)methanone |
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Frequently Asked Questions
The presence of two iodine atoms significantly increases molecular weight and polarizability, while the phenolic –OH group provides a reactive hydrogen-bond donor site. This compound features a benzofuran core substituted with a butyl chain at the 2-position, enhancing hydrophobic character, and a 4-hydroxy-3,5-diiodophenyl moiety connected through a ketone (carbonyl) linkage.
The CAS number of (2-Butylbenzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) ketone is 1951-26-4.
The molecular formula of (2-Butylbenzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) ketone is C19H16I2O3.
The listed molecular weight of (2-Butylbenzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) ketone is 546.1 g/mol.
(2-Butylbenzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) ketone is listed as being used in connection with the following API: Amiodarone.
The listed synonym or IUPAC name for (2-Butylbenzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) ketone is (2-butyl-1-benzofuran-3-yl)-(4-hydroxy-3,5-diiodophenyl)methanone.