|
| tert-Butyl O,O-dimethylphosphonoacetate Basic information |
Product Name: | tert-Butyl O,O-dimethylphosphonoacetate | Synonyms: | tert-Butyl P,P-diMethylphosphonoacetate, >= 97.0 % GC;tert-Butyl ((oxo)dimethoxyphosphino)acetate;tert-Butyl (dimethoxyphosphinyl)acetate;tert-Butyl 2-(dimethoxyphosphoryl);Tert-butyl dimethylphosphonoactate;Dimethyl (Boc-methyl)phosphonate;TERT-BUTYL P,P-DIMETHYLPHOSPHONOACETATE;tert-Butyl O,O-dimethylphosphonoacetate | CAS: | 62327-21-3 | MF: | C8H17O5P | MW: | 224.19 | EINECS: | | Product Categories: | | Mol File: | 62327-21-3.mol | |
| tert-Butyl O,O-dimethylphosphonoacetate Chemical Properties |
Boiling point | 86-87 °C0.02 mm Hg(lit.) | density | 1.131 g/mL at 20 °C(lit.) | refractive index | n20/D 1.434 | Fp | 110 ºC | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | form | clear liquid | color | Colorless to Almost colorless | BRN | 4861886 |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26 | WGK Germany | 3 | F | 9-23 | HS Code | 2931.39.0030 |
| tert-Butyl O,O-dimethylphosphonoacetate Usage And Synthesis |
Uses | Reactant for:
- Preparation of phosphonate terminated PPH dendrimers as anti-HIV-1 agents
- Preparation of monodehydro diketopiperazines from ketoacyl amino acid amides via acid-catalyzed cyclization
- Preparation of α,β-unsaturated esters for use in the guanidine-catalyzed oxa-Michael addition
- Preparation of myxopyronin B and desmethyl myxopyronin B analogs, with antibacterial activity and inhibitory activity against bacterial RNA polymerase
- Allylation and subsequent ring-closing metathesis in presence of Grubbs′ catalyst or intramolecular rhodium-catalyzed cyclopropanation reactions
|
| tert-Butyl O,O-dimethylphosphonoacetate Preparation Products And Raw materials |
|