Chemistry:Diisopropyl azodicarboxylate
From HandWiki
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| Names | |
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| IUPAC name
Diisopropyl azodicarboxylate
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| Other names
DIAD
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C8H14N2O4 | |
| Molar mass | 202.210 g·mol−1 |
| Appearance | Orange liquid |
| Density | 1.027 g/cm3 |
| Melting point | 3 to 5 °C (37 to 41 °F; 276 to 278 K) |
| Boiling point | 75 °C (167 °F; 348 K) at 0.25 mmHg |
| insoluble | |
Refractive index (nD)
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1.418-1.422 |
| Hazards | |
| Safety data sheet | Sigma-Aldrich |
| GHS pictograms |   
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| GHS Signal word | Warning |
| H315, H319, H335, H373, H411 | |
| P260, P261, P264, P271, P273, P280, P302+352, P304+340, P305+351+338, P312, P314, P321, P332+313, P337+313, P362, P391, P403+233, P405, P501 | |
| Flash point | 106 °C (223 °F; 379 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Diisopropyl azodicarboxylate (DIAD) is the diisopropyl ester of azodicarboxylic acid. It is used as a reagent in the production of many organic compounds. It is often used in the Mitsunobu reaction,[1] where it serves as an oxidizer of triphenylphosphine to triphenylphosphine oxide. It has also been used to generate aza-Baylis-Hillman adducts with acrylates.[2] It can also serve as a selective deprotectant of N-benzyl groups in the presence of other protecting groups.[3]
It is sometimes preferred to diethyl azodicarboxylate (DEAD) because it is more hindered, and thus less likely to form hydrazide byproducts.
One notable use of this compound is in the synthesis of Bifenazate (Floramite®).[citation needed]
References
- ↑ "luka DIAD on Sigma-Aldrich". https://www.sigmaaldrich.com/catalog/search/ProductDetail/FLUKA/11626. Retrieved 2008-11-18.
- ↑ Shi, Min; Zhao, Gui-Ling (2004). "Aza-Baylis–Hillman reactions of diisopropyl azodicarboxylate or diethyl azodicarboxylate with acrylates and acrylonitrile". Tetrahedron 60 (9): 2083–2089. doi:10.1016/j.tet.2003.12.059.
- ↑ Kroutil, J.; Trnka, T.; Cerny, M. (2004). "Improved procedure for the selective N-debenzylation of benzylamines by diisopropyl azodicarboxylate". Synthesis 3 (3): 446–450. doi:10.1055/s-2004-815937.
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