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| | TERT-BUTYL N-(BENZYLOXY)CARBAMATE Basic information |
| | TERT-BUTYL N-(BENZYLOXY)CARBAMATE Chemical Properties |
| Melting point | 45-47 °C (lit.) | | density | 1.078±0.06 g/cm3 (20 ºC 760 Torr) | | storage temp. | Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Ethyl Acetate (Slightly) | | form | Solid | | color | White | | InChIKey | MZNBNPWFHGWAGH-UHFFFAOYSA-N | | CAS DataBase Reference | 79722-21-7 |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | HS Code | 29280000 |
| | TERT-BUTYL N-(BENZYLOXY)CARBAMATE Usage And Synthesis |
| Chemical Properties | White powder | | Uses | tert-Butyl N-(Benzyloxy)carbamate has been used in the synthesis of Deferoxamine Mesylate (D228980), an iron chelating agent used in therapy for patients with sickle cell diseases and iron overload. Studies suggest that it can exert potential antioxidant neuroprotective effects in stroke patients | | Uses | tert-Butyl N-(benzyloxy)carbamate was used in the preparation of seven-membered cyclic hydroxamic acids. It may be used in the synthesis of 2-(N-formyl-N-hydroxyamino) ethylphosphonate (IPP). | | General Description | tert-Butyl N-(benzyloxy)carbamate (tert-butyl benzyloxycarbamate), a protected hydroxylamine, is an N-alkyl-N-benzyloxy carbamate. Its C-N cross coupling reaction with fluorescein ditriflate has been reported. It participates in facile intramolecular cyclization with various carbon nucleophiles to afford functionalized 5- and 6-membered protected cyclic hydroxamic acids. |
| | TERT-BUTYL N-(BENZYLOXY)CARBAMATE Preparation Products And Raw materials |
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