CAS:108957-20-6 N-BOC-3-IODO-L-ALANINE BENZYL ESTER
NAME:N-BOC-3-IODO-L-ALANINE BENZYL ESTER CAS:108957-20-6 MF:C15H20INO4 MW:405.23 PURITY:98%
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Material Chemistry
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Product introduction
| NAME | N-BOC-3-IODO-L-ALANINE BENZYL ESTER |
| CAS | 108957-20-6 |
| MF | C15H20INO4 |
| MW | 405.23 |
| EINECS | 200-258-5 |
| MP | 78-80 °C |
| BP | 460.1±40.0 °C |
| STORAGE | 2-8°C |
Description
Synthesis Analysis
The synthesis of Boc-protected amino acid derivatives typically involves the protection of the amino group with a Boc group, followed by the introduction of other substituents such as iodine. While the exact synthesis of "N-Boc-3-Iodo-L-alanine benzyl ester" is not detailed in the provided papers, similar compounds, such as N-Boc-3-amino-tyrosine methyl ester, have been synthesized using methods that could potentially be adapted for the synthesis of the target compound . The conventional 1,3-dicyclohexylcarbodiimide (DCC) and 1-hydroxybenzotriazole (HOBt) protocol is a common coupling method used in the synthesis of Boc-protected amino acid esters, as seen in the preparation of N-para-ferrocenyl benzoyl dipeptide esters
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