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Diisopropyl azodicarboxylate
[CAS# 2446-83-5]

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Identification
Classification Chemical reagent >> Organic reagent >> Ester >> Propyl esters
Name Diisopropyl azodicarboxylate
Synonyms DIAD
Molecular Structure CAS # 2446-83-5, Diisopropyl azodicarboxylate, DIAD
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
Properties
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
Safety Data
Hazard Symbols symbol symbol   GHS07;GHS08 Warning    Details
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
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Specific target organ toxicity - single exposureSTOT SE3H335
Specific target organ toxicity - repeated exposureSTOT RE2H373
CarcinogenicityCarc.2H351
Specific target organ toxicity - single exposureSTOT SE3H371
Transport Information UN 3082
SDS Available
up Discovory and Applicatios
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
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