Name | bromodifluoromethane diethyl phosphate |
Synonyms | Bromodifluoromethyl diethylphosphonate BROMODIFLUOROMETHANE DIETHYL PHOSPHATE bromodifluoromethane diethyl phosphate BROMODIFLUOROMETHYL DIETHYLPHOSPHONATE Diethyl bromodifluoromethanephosphonate Bromodifluoromethyl diethyl phosphonate Diethyl (bromodifluoromethyl)phosphonate DIETHYL (BROMODIFLUOROMETHYL)PHOSPHONATE Bromodifluoromethyl diethyl phosphonate~Diethyl bromodifluoromethanephosphonate BromodifluoromethylphosphonicAcidDiethylEsterDiethylBromodifluoromethylphosphonate |
CAS | 65094-22-6 |
InChI | InChI=1/C5H10BrF2O3P/c1-3-10-12(9,11-4-2)5(6,7)8/h3-4H2,1-2H3 |
Molecular Formula | C5H10BrF2O3P |
Molar Mass | 267.01 |
Density | 1.503 g/mL at 25 °C (lit.) |
Boling Point | 40-41 °C/0.05 mmHg (lit.) |
Flash Point | >230°F |
Water Solubility | Not miscible or difficult to mix in water. |
Solubility | Chloroform, Ethyl Acetate |
Vapor Presure | 0.58mmHg at 25°C |
Appearance | liquid |
Specific Gravity | 1.503 |
Color | colorless |
BRN | 1944045 |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Refractive Index | n20/D 1.417(lit.) |
Hazard Symbols | Xi - Irritant |
Risk Codes | R21/22 - Harmful in contact with skin and if swallowed. R36/38 - Irritating to eyes and skin. R38 - Irritating to the skin R36 - Irritating to the eyes |
Safety Description | 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. S60 - This material and its container must be disposed of as hazardous waste. S37 - Wear suitable gloves. S23 - Do not breathe vapour. |
UN IDs | 3278 |
WGK Germany | 3 |
TSCA | No |
HS Code | 29319090 |
Hazard Note | Irritant |
Hazard Class | IRRITANT, IRRITANT-H |
Packing Group | III |
Introduction | diethyl bromofluoromethylphosphonate has the molecular formula C5H10BrF2O3P. The widespread use of fluorine-containing compounds has greatly promoted the development of methods for introducing fluorine atoms and fluorine-containing groups into organic molecules. At present, the method of trifluoromethylation has been fully studied, while the development of other fluoroalkylation is relatively lagging behind, although the widespread use of fluorine-containing compounds has greatly promoted the development of methods for introducing fluorine atoms and fluorine-containing groups into organic molecules. |
Application | diethyl Bromo fluoromethylphosphonate is an ester organic compound, which can be used as an intermediate in organic synthesis. |