54829-48-0 Usage
Uses
Used in Pharmaceutical Industry:
2-Iodofuran is utilized as a building block in organic synthesis for its potential in the development of new pharmaceuticals. Its iodine atom facilitates a range of chemical reactions, such as substitution, coupling, and metal-catalyzed processes, which are crucial for creating novel drug molecules.
Used in Agrochemical Development:
Beyond pharmaceuticals, 2-Iodofuran also shows promise in the creation of new agrochemicals, leveraging its unique structure and reactivity to enhance the properties of agricultural chemicals.
Used in Organic Chemistry Research:
As a reagent of interest in the field of organic chemistry, 2-Iodofuran is employed by researchers and professionals in medicinal chemistry and material science to explore its properties and applications, contributing to the advancement of chemical knowledge and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 54829-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,2 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54829-48:
(7*5)+(6*4)+(5*8)+(4*2)+(3*9)+(2*4)+(1*8)=150
150 % 10 = 0
So 54829-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H3IO/c5-4-2-1-3-6-4/h1-3H
54829-48-0Relevant academic research and scientific papers
Regiospecific Synthesis of Aryl(2-furyl)iodonium Tosylates, a New Class of Iodonium Salts, from arenes and 2-(Trimethylsilyl)furans in Organic Solvents
Carman, Carol S.,Koser, Gerald F.
, p. 2534 - 2539 (2007/10/02)
The treatment of 2,5-bis(trimethylsilyl)furan with various arenes (ArI(OH)OTs) in acetonitrile/ methanol has been found to give aryliodonium tosylates in yields ranging from 62percent to 80percent.With 2-methyl-5-(trimethylsilyl)furan as the substrate, aryl(5-methyl-2-furyl)iodonium tosylates are likewise obtained in yields ranging from 61percent to 74percent.The reactions of arenes with 2-(trimethylsilyl)furan in methanol give aryl(2-furyl)iodonium tosylates in much lower yield (9-23percent) and are accompanied by the reductive decomposition of the hypervalent organoiodine component.To our knowledge, these are the first reported examples of aryl(furyl)iodonium salts.
