Molecular structure of Acetyl Iodide, CAS Number: 507-02-8
Acetyl Iodide (CAS 507-02-8)
Alternate Names:
acetyliodid
Application:
Acetyl Iodide is an ether used in organic synthesis
CAS Number:
507-02-8
Molecular Weight:
169.95
Molecular Formula:
C2H3IO
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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Acetyl iodide is a reactive organic compound in various chemical reactions. It is as an acetylating agent in organic synthesis, particularly in the acetylation of alcohols and amines. Acetyl iodide its ability to efficiently acetylate a wide range of functional groups, making it versatile in the modification of organic molecules. In biochemistry, acetyl iodide plays a role in the synthesis of complex organic molecules, enabling the modification of specific functional groups to achieve desired chemical properties. Its reactivity and selectivity make it a reagent in the field of organic chemistry.
Acetyl Iodide (CAS 507-02-8) References
- Syntheses of allene-modified derivatives of peridinin toward elucidation of the effective role of the allene function in high energy transfer efficiencies in photosynthesis. | Kajikawa, T., et al. 2009. Org Biomol Chem. 7: 3723-33. PMID: 19707676
- Frontiers, opportunities, and challenges in biochemical and chemical catalysis of CO2 fixation. | Appel, AM., et al. 2013. Chem Rev. 113: 6621-58. PMID: 23767781
- Hexabromo- and hexaiododisilane: small and simple molecules showing completely different crystal structures. | Berger, M., et al. 2014. Acta Crystallogr C Struct Chem. 70: 1088-91. PMID: 25370113
- A chemical biology route to site-specific authentic protein modifications. | Yang, A., et al. 2016. Science. 354: 623-626. PMID: 27708052
- X-ray Absorption Spectroscopy Reveals an Organometallic Ni-C Bond in the CO-Treated Form of Acetyl-CoA Synthase. | Can, M., et al. 2017. Biochemistry. 56: 1248-1260. PMID: 28186407
- A new route to synthesize aryl acetates from carbonylation of aryl methyl ethers. | Mei, Q., et al. 2018. Sci Adv. 4: eaaq0266. PMID: 29795781
- Catalytic Generation and Use of Ketyl Radical from Unactivated Aliphatic Carbonyl Compounds. | Seo, H. and Jamison, TF. 2019. Org Lett. 21: 10159-10163. PMID: 31820654
- Application of Coordination Compounds with Transition Metal Ions in the Chemical Industry-A Review. | Malinowski, J., et al. 2020. Int J Mol Sci. 21: PMID: 32751682
- Recent advances in the chemistry of ketyl radicals. | Péter, Á., et al. 2021. Chem Soc Rev. 50: 5349-5365. PMID: 33972956
- Isolating reactive metal-based species in Metal-Organic Frameworks - viable strategies and opportunities. | Young, RJ., et al. 2020. Chem Sci. 11: 4031-4050. PMID: 34122871
- Potassium Iodide Nanoparticles Enhance Radiotherapy against Breast Cancer by Exploiting the Sodium-Iodide Symporter. | Cline, BL., et al. 2021. ACS Nano. 15: 17401-17411. PMID: 34694109
- 1-Aminoalkylphosphonium Derivatives: Smart Synthetic Equivalents of N-Acyliminium-Type Cations, and Maybe Something More: A Review. | Adamek, J., et al. 2022. Molecules. 27: PMID: 35268663
- Excited-State Dynamics during Primary C-I Homolysis in Acetyl Iodide Revealed by Ultrafast Core-Level Spectroscopy. | Troß, J., et al. 2023. J Phys Chem A. 127: 4103-4114. PMID: 37103479
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Acetyl Iodide, 5 g | sc-396846 | 5 g | $739.00 |