Molecular Formula | C10H5F6IO4 |
Molar Mass | 430.04 |
Density | 1.95g/cm3 |
Melting Point | 121-125°C(lit.) |
Boling Point | 267.573°C at 760 mmHg |
Flash Point | 115.624°C |
Water Solubility | insoluble |
Solubility | Chloroform (Slightly), Dichloromethane (Slightly), DMSO (Slightly) |
Vapor Presure | 0.008mmHg at 25°C |
Appearance | Crystalline powder |
Color | White to pale yellow |
BRN | 764767 |
Storage Condition | Keep in dark place,Inert atmosphere,2-8°C |
Stability | Air and Moisture Sensitive |
Sensitive | Moisture & Light Sensitive |
Refractive Index | 1.483 |
MDL | MFCD00009672 |
Use | Used for α-hydroxylation of ketones under acidic conditions, and also used for fluorination reagents. |
Hazard Symbols | Xi - Irritant![]() |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection |
WGK Germany | 3 |
FLUKA BRAND F CODES | 4.10-8-9-21 |
HS Code | 29036990 |
Hazard Note | Irritant/Keep Cold |
Hazard Class | IRRITANT, KEEP COLD, |
Use | Used as a multifunctional oxidant; Under acidic conditions, it is used for the direct α-hydroxylation reaction of ketones; In the presence of HF pyridine, it is used as p-fluorinated reagent for 4-alkylphenol, used to synthesize 4-fluorocyclohexane-2, 5-dienone; used for N-acylhydrazone to produce 1,3, 4-Oxadiazole oxidation reaction reagent; used to promote the cyclization reaction of styrylamine to N-alkyl or N-arylindole; dehydrogenation reaction and oxidation reaction reagent; direct conversion of amide to amines (Hoffman Rearrangement) is a new reagent, a key substance for the ordering of carboxyl-terminal peptides; a reagent for desulfurization and acetalization to carbonyl |
production method | 1.?1.485 grams (5.41 mmol) of iodobenzene dichloride was added to 2.39 grams (10.8 mmol) of potassium trifluoroacetate in a solution of 17 ml of silver. Filtered, the product obtained by lyophilizing the filtrate contains a trace of silver trifluoroacetate. 2. 2g iodobenzene and 4 ml of resteamed trifluoroacetic acid were heated on a water vapor bath for 45 minutes. Pour into ether (50ml), evaporate part of the ether to precipitate yellow and white crystals, and wash with a small amount of ether to wash off the color. 3.20g of diacetic acid iodobenzene is dissolved in 30 ml of hot trifluoroacetic acid to obtain 15g (53%). Bis (trifluoroacetic acid) iodobenzene is crystallized. The first part is dried in a solid sodium hydroxide dryer, which is pure enough. This compound can be recrystallized from acetone-petroleum ether and then cooled to 0 ℃. Another product can be obtained, but it contains diacetate and is seriously impure. In addition, there is a method for electrophilic substitution of tris (difluoroacetic acid) iodine and benzene |