Date published: 2026-4-25

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Iodomesitylene Diacetate (CAS 33035-41-5)

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Alternate Names:
2-(Diacetoxyiodo)mesitylene; 2,4,6-Trimethyl(diacetoxyiodo)benzene
CAS Number:
33035-41-5
Molecular Weight:
364.18
Molecular Formula:
C13H17IO4
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Iodomesitylene Diacetate, referred to as TDI, holds significant prominence in scientific research applications. Iodomesitylene Diacetate serves as a intermediate in the synthesis of various compounds and has found extensive utilization as a reagent in the production of agrochemicals, and dyes. The applications of Iodomesitylene Diacetate in scientific research are diverse and encompass several domains. Furthermore, Iodomesitylene Diacetate has played a role in the synthesis of polymers, notably contributing to the formation of polyurethanes and polyesters. Additionally, its catalytic properties have been harnessed in the synthesis of heterocyclic compounds. Iodomesitylene Diacetate functions as an electrophilic reagent during the synthesis of various compounds. It readily engages with nucleophiles such as alcohols, amines, and carboxylic acids, initiating a reaction that culminates in the formation of a product. The process commences with the generation of a carbocation, which subsequently undergoes reaction with the nucleophile to yield the desired product.


Iodomesitylene Diacetate (CAS 33035-41-5) References

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  4. Unsymmetrical Aryl(2,4,6-trimethoxyphenyl)iodonium Salts: One-Pot Synthesis, Scope, Stability, and Synthetic Studies.  |  Seidl, TL., et al. 2016. J Org Chem. 81: 1998-2009. PMID: 26828570
  5. Decarboxylative sp3 C-N coupling via dual copper and photoredox catalysis.  |  Liang, Y., et al. 2018. Nature. 559: 83-88. PMID: 29925943
  6. Mechanistic Study on the Decarboxylative sp3 C-N Cross-Coupling between Alkyl Carboxylic Acids and Nitrogen Nucleophiles via Dual Copper and Photoredox Catalysis.  |  Zhao, X., et al. 2019. Inorg Chem. 58: 12669-12677. PMID: 31498616
  7. Effect of the Ligand Backbone on the Reactivity and Mechanistic Paradigm of Non-Heme Iron(IV)-Oxo during Olefin Epoxidation.  |  Biswas, JP., et al. 2021. Angew Chem Int Ed Engl. 60: 14030-14039. PMID: 33836110
  8. Metallaphotoredox: The Merger of Photoredox and Transition Metal Catalysis.  |  Chan, AY., et al. 2022. Chem Rev. 122: 1485-1542. PMID: 34793128
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  10. Recent developments in decarboxylative cross-coupling reactions between carboxylic acids and N-H compounds.  |  Arshadi, S., et al. 2019. RSC Adv. 9: 8964-8976. PMID: 35517670
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Iodomesitylene Diacetate, 5 g

sc-295187
5 g
$213.00

Iodomesitylene Diacetate, 10 g

sc-295187A
10 g
$379.00