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| | TRIS(TRIMETHYLSILYL)PHOSPHITE Basic information |
| | TRIS(TRIMETHYLSILYL)PHOSPHITE Chemical Properties |
| Boiling point | 78-81 °C/8 mmHg (lit.) | | density | 0.893 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.409(lit.) | | Fp | >230 °F | | form | Liquid | | Specific Gravity | 0.893 | | color | Clear colorless | | Water Solubility | Sparingly soluble in water. | | Sensitive | Air & Moisture Sensitive | | Hydrolytic Sensitivity | 8: reacts rapidly with moisture, water, protic solvents | | BRN | 2043814 | | InChI | InChI=1S/C9H27O3PSi3/c1-14(2,3)10-13(11-15(4,5)6)12-16(7,8)9/h1-9H3 | | InChIKey | VMZOBROUFBEGAR-UHFFFAOYSA-N | | SMILES | [Si](C)(C)(OP(O[Si](C)(C)C)O[Si](C)(C)C)C | | CAS DataBase Reference | 1795-31-9(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/38 | | Safety Statements | 26-36 | | RIDADR | 1760 | | WGK Germany | 3 | | F | 10-21 | | TSCA | No | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29319000 |
| | TRIS(TRIMETHYLSILYL)PHOSPHITE Usage And Synthesis |
| Uses | Tris(trimethylsilyl) Phosphite is used in the studies of bisphosphonic acids as effective inhibitor of glutamine synthetase, a promising approach for the discovery of novel drugs against tuberculosis. It also acts as a reagent in the preparation of substituted calix[4]arenes bearing one or two α-hydroxymethylphosphonic acid fragments at upper rim of macrocycle as inhibitors of glutathione S-transferase in vitro. |
| | TRIS(TRIMETHYLSILYL)PHOSPHITE Preparation Products And Raw materials |
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