Other grades of this product :
| BREDERECK'S REAGENT Basic information |
| BREDERECK'S REAGENT Chemical Properties |
| Boiling point | 50-55 °C/15 mmHg (lit.) | | density | 0.844 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.422(lit.) | | Fp | 106 °F | | storage temp. | Sealed in dry,Store in freezer, under -20°C | | form | Liquid | | pka | 5.46±0.38(Predicted) | | Specific Gravity | 0.844 | | color | Clear pale yellow | | BRN | 1901973 | | InChIKey | HXRAMSFGUAOAJR-UHFFFAOYSA-N | | CAS DataBase Reference | 5815-08-7(CAS DataBase Reference) |
| Hazard Codes | Xi,F | | Risk Statements | 10-36/37/38 | | Safety Statements | 26 | | RIDADR | UN 1993 3/PG 3 | | WGK Germany | 3 | | F | 10 | | HazardClass | 3 | | PackingGroup | III | | HS Code | 29221990 |
| BREDERECK'S REAGENT Usage And Synthesis |
| Chemical Properties | Clear pale yellow liquid | | Uses | Reactant for:• ;Preparation of pyrroloquinazolines as photochemotherapeutic agents1• ;Enanatioslective formal synthesis of the Cinchona alkaloid quinine via stereoselective intermolecular radical addition2• ;Synthesis of camptothecin via intramolecular isomuenchnone cycloaddition reaction3• ;Aminomethylenation reactions4 | | Uses | Mild enamination reagent; catalyst in ring-opening polymerization reactions. | | Uses | Reactant for:- Preparation of pyrroloquinazolines as photochemotherapeutic agents
- Enanatioslective formal synthesis of the Cinchona alkaloid quinine via stereoselective intermolecular radical addition
- Synthesis of camptothecin via intramolecular isomuenchnone cycloaddition reaction
- Aminomethylenation reactions
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| BREDERECK'S REAGENT Preparation Products And Raw materials |
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