Name | Triethyl 2-phosphonopropionate |
Synonyms | TRIETHYL 2-PHOSPHONOPROPIONATE Triethyl 2-phosphonopropionate ETHYL-2-(DIETHYLPHOSPHONO)PROPANOATE ethyl 2-(diethoxyphosphoryl)propanoate DIETHYL ETHOXYCARBONYLETHYL-PHOSPHONATE 2-Phosphonopropionic acid triethyl ester 2-phosphonopropionic acid triethyl ester ethyl (2S)-2-(diethoxyphosphoryl)propanoate diethyl 1-(ethoxycarbonyl)ethanephosphonate Diethyl 1-(ethoxycarbonyl)ethanephosphonate ethyl (2R)-2-(diethoxyphosphoryl)propanoate 2-DIETHYLPHOSPHONOPROPIONIC ACID ETHYL ESTER Diethyl 1-(ethoxycarbonyl)ethanephosphonate~2-Phosphonopropionic acid triethyl ester |
CAS | 3699-66-9 |
EINECS | 223-033-4 |
InChI | InChI=1/C9H19O5P/c1-5-12-9(10)8(4)15(11,13-6-2)14-7-3/h8H,5-7H2,1-4H3/t8-/m0/s1 |
InChIKey | BVSRWCMAJISCTD-UHFFFAOYSA-N |
Molecular Formula | C9H19O5P |
Molar Mass | 238.22 |
Density | 1.111g/mLat 25°C(lit.) |
Melting Point | 161-164° |
Boling Point | 143-144°C12mm Hg(lit.) |
Flash Point | 192°F |
Solubility | Miscible with chloroform and methanol. |
Vapor Presure | 0.00507mmHg at 25°C |
Appearance | Liquid |
Specific Gravity | 1.111 |
Color | Clear colorless |
BRN | 1786994 |
Storage Condition | Inert atmosphere,Room Temperature |
Refractive Index | n20/D 1.431(lit.) |
MDL | MFCD00009159 |
Use | Wittig-Horner reagent, widely used in the reaction of aldehydes and ketones to form acrylic acid. |
Hazard Symbols | Xi - Irritant |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R38 - Irritating to the skin R37 - Irritating to the respiratory system R36 - Irritating to the eyes |
Safety Description | S23 - Do not breathe vapour. S24/25 - Avoid contact with skin and eyes. S36 - Wear suitable protective clothing. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S39 - Wear eye / face protection. S37 - Wear suitable gloves. |
UN IDs | 1993 |
WGK Germany | 3 |
FLUKA BRAND F CODES | 10 |
HS Code | 29319019 |
Hazard Note | Irritant |
Use | Used for intramolecular conjugate addition reaction to synthesize floresolide B, chemical enzyme one-pot method to synthesize γ-butyrolactone, through asymmetric hydrogenation reaction, Enantioselective synthesis of spiro dihydroindene dimethyl acetic acid, stereoselective intramolecular Diels-Alder reaction and Horner-Wadsworth-Emmons reaction; it can undergo condensation reaction with various aldehydes and ketones to form acrylate |