| CAS | 2449-05-0 |
|---|---|
| Synonyms | AKOS024348901 | NCI60_006088 | Q27285524 | Dibenzyl azodicarboxylate | benzyl N-phenylmethoxycarbonyliminocarbamate | FT-0624649 | IRJKSAIGIYODAN-UHFFFAOYSA-N | DTXSID3044887 | IRJKSAIGIYODAN-ISLYRVAYSA-N | C93451 | Dibenzyl (E)-1,2-diazenedicarboxylate | |
| Specifications & Purity | ≥94% |
| Application | Dibenzyl azodicarboxylate was used as electrophilic reagent in the synthesis of C-glycosyl α-amino acids via proline-catalyzed α-amination of C-glycosylalkyl aldehydes. It was used in enantioselective synthesis of optically active pyrazolidine derivatives |
| Storage | Store at 2-8°C |
| Shipped In | Wet ice |
| Product Description | Dibenzyl azodicarboxylate undergoes[4+2] cycloaddition reaction with glycal to yield 2-aminoglycosides. |
| Pubchem Sid | 504754962 |
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504754962 |
| Mdl Number | MFCD00016737 |
| EC Number | 219-508-0 |
| PubChem CID | 75557 |
| Molecular Formula | C16H14N2O4 |
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