Name | Iodobenzene diacetate |
Synonyms | PIA DAIB AURORA KA-6690 diacetoxyiodo-benzen Iodobenzene diacetate PHENYLIODINE DIACETATE (Diacetoxyiodo)benzene DIACETOXYIODOSOBENZENE (DIACETOXYIODO)BENZENE LABOTEST-BB LT00847235 Iodosobenzene diacetate IODOBENZENE I,I-DIACETATE iodosylbenzene di(acetate) Phenyliodine(III) diacetate bis(acetyloxy)(phenyl)-lambda~3~-iodane |
CAS | 3240-34-4 |
EINECS | 221-808-1 |
InChI | InChI=1/C6H5I.2C2H4O2/c7-6-4-2-1-3-5-6;2*1-2(3)4/h1-5H;2*1H3,(H,3,4) |
InChIKey | ZBIKORITPGTTGI-UHFFFAOYSA-N |
Molecular Formula | C10H11IO4 |
Molar Mass | 322.1 |
Density | 1.6865 (estimate) |
Melting Point | 161-163 °C (lit.) |
Boling Point | 456.8°C at 760 mmHg |
Flash Point | 230.1°C |
Water Solubility | INSOLUBLE |
Solubility | INSOLUBLE |
Vapor Presure | 3.87E-09mmHg at 25°C |
Appearance | White crystal |
Color | Clear to cloudy colorless to yellow |
BRN | 1879369 |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Stability | Light and Moisture sensitive |
Sensitive | Light Sensitive |
Refractive Index | n/D 1.444 |
MDL | MFCD00008692 |
Physical and Chemical Properties | MP 161-165°C |
Use | Used as an intermediate of topotecan |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S37/39 - Wear suitable gloves and eye/face protection S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S27 - Take off immediately all contaminated clothing. |
UN IDs | 1479 |
WGK Germany | 3 |
RTECS | DA3525000 |
FLUKA BRAND F CODES | 4.10-8 |
TSCA | Yes |
HS Code | 29310095 |
Hazard Note | Irritant |
Hazard Class | 6.1(b) |
Packing Group | III |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
traits | white to off-white crystalline powder. |
application | iodophenyl diacetic acid is used in pharmaceutical and other industries. it has good selective oxidation characteristics and has been more and more widely used in recent years. For example, the latest oral lung cancer treatment drug topotecan, the anti-inflammatory analgesic naproxen, the antidepressant fluoxetine, and the influenza drug oseltamivir (Tamiflu) to deal with avian influenza, and the synthesis of anti-tumor drug Aranorosin. It is also used for Hoffman degradation, such as unnatural amino acids L-2, 3-diaminopropionic acid, L-2, the synthesis of 4-diaminobutyric acid, the catalytic halogenation, the ring formation of heterocyclic compounds such as benzimidazole, the oxidation of phenol, the oxidation reaction of porphyrin, etc., the product has a wide range of uses, stable properties, easy to store, and the reaction The by-product is usually the more expensive organic raw material iodobenzene, which can be recycled and recycled, and can also be used to synthesize other compounds without polluting the environment. It is a very ideal oxidation reagent. |
Preparation method | Method 1: A preparation method of iodophenyl diacetic acid, this method uses sodium perborate tetrahydrate as raw material, in the presence of glacial acetic acid/acetic anhydride mixture Acylation reaction with iodobenzene, in which the molar ratio of sodium perborate tetrahydrate to iodobenzene is 3-10: 1, and the reaction temperature is 30 ℃ -45 ℃, the reaction time is 4-24 hours. After the reaction is over, ice water is added to obtain crude iodiphenyl diacetic acid, and then recrystallized to obtain iodiphenyl diacetic acid. Method 2: Efficient and environmentally friendly preparation method of iodophenyl diacetic acid: using iodobenzene as the starting material, acetic acid as the solvent, reacting with peracetic acid, adding water to precipitate iodophenyl diacetic acid. Specifically, it includes: adding iodobenzene and acetic acid to the reaction bottle, controlling the temperature to 30-40 ℃, adding peracetic acid dropwise, stirring for 5 hours after dropping, cooling to 5-10 ℃, centrifuging, washing the filter cake with water and n-heptane in turn, and drying to obtain iodophenyl diacetic acid. |
Use | Used as topotecan intermediate Mild oxidant Biochemical research Multifunctional oxidation and acetic acid reagent; In the reaction of TEMPO oxidizing nerol to neraldehyde, the oxidizing agent is stoichiometric; the oxidizing agent in the azirylation reaction of alkene and sulfamate catalyzed by rhodium; used for palladium-catalyzed 2-arylation of indole at room temperature; used for the synthesis of a wide variety of heterocyclic compound reagents; vic-ethylene glycol lysating agent, hydroxylation and many oxidation reactions; used for the preparation of thermally unstable substances Iodine benzene Rhodium-catalyzed olefin azacyclic propane sulfonate oxidant. A useful reagent for the synthesis of various heterocyclic compounds using palladium-catalyzed 2-arylation of indole at room temperature. |