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| Classification | Chemical reagent >> Organic reagent >> Ester >> Propyl esters |
|---|---|
| Name | Diisopropyl azodicarboxylate |
| Synonyms | DIAD |
| Molecular Structure | ![]() |
| Molecular Formula | C8H14N2O4 |
| Molecular Weight | 202.21 |
| CAS Registry Number | 2446-83-5 |
| EC Number | 219-502-8 |
| SMILES | CC(C)OC(=O)/N=N/C(=O)OC(C)C |
| Density | 1.02 |
|---|---|
| Melting point | 3-5 ºC |
| Boiling point | 75 ºC (0.2 mmHg) |
| Refractive index | 1.418-1.422 |
| Flash point | 106 ºC |
| Water solubility | insoluble |
| Hazard Symbols |
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| Hazard Statements | H315-H319-H335-H373-H411 Details | ||||||||||||||||||||||||||||||||||||
| Precautionary Statements | P260-P261-P264-P264+P265-P271-P273-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P391-P403+P233-P405-P501 Details | ||||||||||||||||||||||||||||||||||||
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| Transport Information | UN 3082 | ||||||||||||||||||||||||||||||||||||
| SDS | Available | ||||||||||||||||||||||||||||||||||||
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Diisopropyl azodicarboxylate (DIAD) is a versatile compound that has had a major impact on organic synthesis since its discovery. First synthesized in 1960 by J. W. Cook and W. R. Benson, DIAD has become a cornerstone reagent in organic chemistry, highly regarded for its efficiency and selectivity in a wide range of reactions.
References 2024. Synthetic studies on the tetrasubstituted D-ring of cystobactamids lead to potent terephthalic acid antibiotics. *Communications Chemistry*, 7(1). DOI: 10.1038/s42004-024-01337-6 2023. (Parallel) kinetic resolution of 3,3-disubstituted indolines via organocatalyzed reactions with azodicarboxylates. *Science China Chemistry*, 66(11). DOI: 10.1007/s11426-023-1810-9 2024. Synthesis of oligosaccharides from terminal B. pertussis LPS pentasaccharide and definition of the minimal epitope recognized by anti-pertussis antibodies. *Glycoconjugate Journal*, 41(3). DOI: 10.1007/s10719-024-10160-z |
| Market Analysis Reports |
| List of Reports Available for Diisopropyl azodicarboxylate |