Name | Methyl diethylphosphonoacetate |
Synonyms | POME Methyl diethylphosphonoacetate Methyl (diethylphosphono)acetate methyl (diethoxyphosphoryl)acetate [3-(methoxycarbonyl)pentan-3-yl]phosphonic acid [(Methoxycarbonyl)-methyl]-phosphonic acid diethyl ester Diethyl methoxycarbonylmethyl phosphonate~Phosphonoacetic acid diethyl methyl ester |
CAS | 1067-74-9 |
EINECS | 213-938-2 |
InChI | InChI=1/C7H15O5P/c1-4-7(5-2,6(8)12-3)13(9,10)11/h4-5H2,1-3H3,(H2,9,10,11) |
Molecular Formula | C7H15O5P |
Molar Mass | 210.165 |
Density | 1.26g/cm3 |
Boling Point | 346.127°C at 760 mmHg |
Flash Point | 163.132°C |
Vapor Presure | 0mmHg at 25°C |
Appearance | Form Liquid, color Clear colorless to fail yellow |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.466 |
Physical and Chemical Properties | NIST Chemical Information Aetic acid, phosphono-, p,p-diethyl c-methyl ester(1067-740-9) |
Use | Uses for an important class of Wittig-horner reagent, can be used as a plasticizer, fire retardant and extractant, etc., is also used in the manufacture of vitamin compounds, drugs, insect pheromones and other natural compounds of the important intermediates. |
Hazard Symbols | Xi - Irritant |
Risk Codes | R36/37/38 - 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. |
WGK Germany | 3 |
FLUKA BRAND F CODES | 10 |
HS Code | 29310095 |
Raw Materials | 反式-2-己烯酸甲酯 |
Downstream Products | METHYL TRANS-2-HEXENOATE |
solubility | Miscible with tetrahydrofuran. |
BRN | 1782397 |
Diethyl phosphonoacetate is a colorless to light yellow transparent liquid, which can be used for the synthesis of branched allyl fluoride; used for regioselective Diels-Alder reactions to generate antibacterial blocks; used for thiophene and furan The synthesis of substituents is used for the treatment of type 2 diabetes; for stereoselective Diels-Alder cycloaddition reactions; for the synthesis of neuroactive pyridone alkaloids.