HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Trimethylsilylmethyl Azide
DK939 · DKSI087 · DKFELEX0251 · RIMETHYLSILYLMETHYL AZIDE · AZIDOMETHYLTRIMETHYLSILANE · Trimethylsilylmethyl azide · Silyl Methyl azide triMethyl · Silane, (azidomethyl)trimethyl-

Identifikatoren & physikalische Daten
| CAS No. | 87576-94-1 |
|---|---|
| Summenformel | C4H11N3Si |
| Durchschnittliche Molmasse | 129,24 g/mol |
| Monoisotopische Masse | 129,07222388 g/mol |
| SMILES | C[Si](C)(C)CN=[N+]=[N-] |
| InChIKey | HKBUFTCADGLKAS-UHFFFAOYSA-N |
| PubChem CID | 150751 |
| EC No. | 677-362-7 |
| DTXSID | DTXSID40236487 |
Chemische & physikalische Eigenschaften
| Polarare Oberfläche (TPSA) | 14,4 |
|---|---|
| H-Brücken-Donoren | 0 |
| H-Brücken-Akzeptoren | 2 |
| Frei drehbare Bindungen | 2 |
| Schwere Atome | 8 |
| Formalladung | 0 |
| Komplexität | 109 |
| Siedepunkt | 92-95°C |
| Dichte | 0,87 g/cm3 |
| Brechungsindex | 1.4300 to 1.4340 |
| Flammpunkt | 6°C |
| Löslichkeit | Sol organic solventsinsol water. |
| Aggregatzustand | clear liquid |
| Farbe | Colorless to Yellow to Green |
| Wichte | 0.87 |
| InChI | InChI=1S/C4H11N3Si/c1-8(2,3)4-6-7-5/h4H2,1-3H3 |
| InChIKey | HKBUFTCADGLKAS-UHFFFAOYSA-N |
| SMILES | C(N=[N+]=[N-])[Si](C)(C)C |
Sicherheit & Vorschriften
| GHS-Einstufung | DangerH225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501 (click each P-code to see the statement)The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory. |
|---|---|
| Hazard Classes and Categories | Flam. Liq. 2 (100%) |
| UN-Transportnummer | 1992 |
| Zollcode | 2931900090 |
| R-Sätze (R) | 11-23/24/25 |
| Sicherheitshinweise (S) | 16-36/37/39-45 |
| Gefahrenklasse | 3 |
| Verpackungsgruppe | II |
Anwendungen & Verwendung
Verwenden
Trimethylsilylmethyl Azide is used in the amination of organometallic compounds; preparation of heterocyclic compounds; precursor of azomethine ylide, reactant in Silylmethyl-Substituted Heterocumulenes and [3 + 2] Cycloaddition etc.
Herstellung & Synthese
synthetische
Obtained in high yield by reaction of sodium azide and (chloromethyl)trimethylsilane in DMF or HMPA at 80°C.