26272-85-5 Usage
Uses
Used in Laboratory Chemicals:
3-IODO-OXETANE is used as a reagent for various laboratory applications, such as the synthesis of other organic compounds and the development of new chemical processes. Its unique properties make it a valuable component in research and development.
Used in Manufacturing of Substances:
3-IODO-OXETANE is used as an intermediate in the production of various substances, contributing to the creation of new materials and compounds with specific properties and applications. Its role in the manufacturing process is essential for the development of innovative products.
Used in Pharmaceutical Industry:
3-IODO-OXETANE can be used as a building block for the synthesis of pharmaceutical compounds, potentially leading to the development of new drugs with improved efficacy and reduced side effects.
Used in Chemical Research:
3-IODO-OXETANE is utilized in chemical research to study its properties and interactions with other compounds, which can lead to a better understanding of its potential applications and the development of new chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 26272-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,7 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26272-85:
(7*2)+(6*6)+(5*2)+(4*7)+(3*2)+(2*8)+(1*5)=115
115 % 10 = 5
So 26272-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H5IO/c4-3-1-5-2-3/h3H,1-2H2
26272-85-5Relevant articles and documents
Visible-Light-Mediated C-I Difluoroallylation with an α-Aminoalkyl Radical as a Mediator
Yue, Fuyang,Dong, Jianyang,Liu, Yuxiu,Wang, Qingmin
supporting information, p. 7306 - 7310 (2021/10/01)
Herein, we report a protocol for direct visible-light-mediated C-I difluoroallylation reactions of α-trifluoromethyl arylalkenes with alkyl iodides at room temperature with an α-aminoalkyl radical as a mediator. The protocol permits efficient functionalization of various α-trifluoromethyl arylalkenes with cyclic and acyclic primary, secondary, and tertiary alkyl iodides and is scalable to the gram level. This mild protocol uses an inexpensive mediator and is suitable for late-stage functionalization of complex natural products and drugs.
Preparation of aryloxetanes and arylazetidines by use of an alkyl-aryl suzuki coupling
Duncton, Matthew A. J.,Estiarte, M. Angels,Tan, Darlene,Kaub, Carl,O'Mahony, Donogh J. R.,Johnson, Russell J.,Cox, Matthew,Edwards, William T.,Wan, Min,Kincaid, John,Kelly, Michael G.
experimental part, p. 3259 - 3262 (2009/05/07)
(Chemical Equation Presented) The oxetan-3-yl and azetidin-3-yl substituents have previously been identified as privileged motifs within medicinal chemistry. An efficient approach to installing these two modules into aromatic systems, using a nickel-mediated alkyl-aryl Suzuki coupling, is presented.
