| 2-(1H-Benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate Chemical Properties | |
| Melting point | 205 °C (dec.)(lit.) |
| storage temp. | 2-8°C |
| solubility | acetonitrile: 0.1 g/mL, clear |
| form | Powder |
| Water Solubility | Soluble in acetonitrile (100 mg/ml, clear, colorless), DMF (160.55 mg/ml, clear), and water (3 mg/ml at 20°C). |
| Sensitive | Moisture Sensitive |
| BRN | 7066325 |
| InChIKey | NQGZJNPFMLJDKU-UHFFFAOYSA-M |
| CAS DataBase Reference | 125700-67-6(CAS DataBase Reference) |
| Safety Information | |
| Hazard Codes | Xi,F,E |
| Risk Statements | 36/37/38-5-2 |
| Safety Statements | 26-36-37/39-36/37/39-35 |
| RIDADR | 1325 |
| WGK Germany | 3 |
| F | 8-10-21 |
| Hazard Note | Irritant/Flammable |
| HazardClass | 4.1 |
| PackingGroup | Ⅱ |
| 2-(1H-Benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate Usage And Synthesis | |
| Chemical Properties | WHITE TO PALE CREAM FINE CRYSTALLINE POWDER |
| Uses | O-(Benzotriazol-1-yl)-N,N,N’N’tetramethyluronium Tetrafluoroborate is used in the synthesis of tetrapeptoid analogues of the antiprotocoal compound Apicidin (A726300). Also used in the synthesis of acid based t-antigen glycodendrimers. |
| Uses | Coupling reagent for peptide synthesis causing low racemization. R. Knorr, A. Trzeciak, W. Bannwarth and D. Gillessen, THL 30, 1927 (1989) |
| 2-(1H-Benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate Preparation Products And Raw materials | |
| Preparation Products | 1-(PIPERIDIN-4-YLCARBONYL)PIPERIDINE |
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