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| TERT-BUTYL 3-BROMOMETHYL-INDOLE-1-CARBOXYLATE Basic information |
| Product Name: | TERT-BUTYL 3-BROMOMETHYL-INDOLE-1-CARBOXYLATE | | Synonyms: | TERT-BUTYL 3-(BROMOMETHYL)-1H-INDOLE-1-CARBOXYLATE;TERT-BUTYL 3-BROMOMETHYL-INDOLE-1-CARBOXYLATE;3-BROMOMETHYL-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER;3-BROMOMETHYL-1-TERT-BUTOXYCARBONYLINDOLE;t-Butyl-3-bromomethylindole-1-carboxylate;3-(Bromomethyl)-1H-indole, N-BOC protected;tert-Butyl 3-(bromomethyl)-1H-indole-1-carboxylate, 3-(Bromomethyl)-1-(tert-butoxycarbonyl)-1H-indole;1-(t-butyloxycarbonyl)-3-(bromomethyl)indole | | CAS: | 96551-21-2 | | MF: | C14H16BrNO2 | | MW: | 310.19 | | EINECS: | | Product Categories: | | Mol File: | 96551-21-2.mol |
| TERT-BUTYL 3-BROMOMETHYL-INDOLE-1-CARBOXYLATE Chemical Properties |
| Melting point | 106 °C | | Boiling point | 391.1±34.0 °C(Predicted) | | density | 1.34±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C |
| TERT-BUTYL 3-BROMOMETHYL-INDOLE-1-CARBOXYLATE Usage And Synthesis |
| Uses | tert-Butyl 3-(bromomethyl)-1H-indole-1-carboxylate is used as a reactant in the preparation of α,α-dialkyl-α-amino acids via enantioselective alkylation of amino acid Schiff bases. |
| TERT-BUTYL 3-BROMOMETHYL-INDOLE-1-CARBOXYLATE Preparation Products And Raw materials |
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