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Energy Chemical |
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| | Diethyl phenylthiomethylphosphonate Basic information |
| Product Name: | Diethyl phenylthiomethylphosphonate | | Synonyms: | Diethyl (phenylsulfanyl)methylphosphonate;Diethyl methylthiobenzyl phosphonate;Phosphonic acid, [(phenylthio)methyl]-, diethyl ester;LABOTEST-BB LT00453966;Diethyl phenylthiomethanephosphonate;NSC 202497;Diethyl[(phenylthio)methyl]phosphonate, 97 %;Phosphonic acid, P-[(phenylthio)methyl]-, diethyl ester | | CAS: | 38066-16-9 | | MF: | C11H17O3PS | | MW: | 260.29 | | EINECS: | 253-770-7 | | Product Categories: | | | Mol File: | 38066-16-9.mol |  |
| | Diethyl phenylthiomethylphosphonate Chemical Properties |
| Boiling point | 146-148 °C (0.5 mmHg) | | density | 1.17 | | refractive index | 1.53-1.533 | | Fp | 146-148°C/0.5mm | | solubility | Difficult to mix. | | form | Liquid | | Specific Gravity | 1.174 | | BRN | 1246215 | | CAS DataBase Reference | 38066-16-9(CAS DataBase Reference) |
| | Diethyl phenylthiomethylphosphonate Usage And Synthesis |
| Chemical Properties | clear light yellow liquid | | Uses | Diethyl phenylthiomethylphosphonate is used to produce Diethylphosphorylmethylphenylsulfoxid, Chemical reagents, pharmaceutical research, pharmaceutical intermediates. | | Application | Diethyl phenylthiomethylphosphonate used for the conversion of aldehydes and ketones to vinyl sulfides, which can be hydrolyzed to yield homologated aldehydes and ketones. | | Preparation | The Arbuzov reaction between phenylthiomethyl chloride (Chloromethyl Phenyl Sulfide) and Triethyl Phosphite is the most commonly used method of preparation (eq 1).
 | | Synthesis Reference(s) | Synthesis, p. 309, 1978 DOI: 10.1055/s-1978-24736 |
| | Diethyl phenylthiomethylphosphonate Preparation Products And Raw materials |
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