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| | BOC-PHE-N(OCH3)CH3 Basic information |
| Product Name: | BOC-PHE-N(OCH3)CH3 | | Synonyms: | BOC-PHE-N(OCH3)CH3;BOC-L-PHENYLALANINE N-METHOXY-N-METHYL AMIDE;N-[(1S)-2-(Methoxymethylamino)-2-oxo-1-(phenylmethyl)ethyl]carbamic Acid 1,1-Dimethylethyl Ester;N-Boc-N-methoxy-N-methyl-L-phenylalaninamide;tert-Butyl [(1S)-1-benzyl-2-[methoxy(methyl)amino]-2-oxoethyl]carbamate;N-Boc-L-phenylalanine N'-Methoxy-N'-MethylaMide;Boc-L-Phe-N(OCH3)CH3;Boc-L-phenylalanineN-methoxy-N-methyl amide≥ 98% (HPLC) | | CAS: | 87694-53-9 | | MF: | C16H24N2O4 | | MW: | 308.37 | | EINECS: | | | Product Categories: | Amino Acids 13C, 2H, 15N;Amino Acids & Derivatives;Chiral Reagents | | Mol File: | 87694-53-9.mol |  |
| | BOC-PHE-N(OCH3)CH3 Chemical Properties |
| storage temp. | Sealed in dry,2-8°C | | solubility | Chloroform, Dichloromethane | | form | Oil | | color | Light Yellow |
| | BOC-PHE-N(OCH3)CH3 Usage And Synthesis |
| Chemical Properties | Light Yellow Oil | | Uses | An intermediate for the synthesis of some HIV protease inhibitors. | | Uses | Reduced by LiAlH4 to give the corresponding Boc amino acid aldehyde. |
| | BOC-PHE-N(OCH3)CH3 Preparation Products And Raw materials |
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