54829-48-0 Usage
General Description
2-Iodofuran is a chemical compound with the molecular formula C4H3IO. It is a heterocyclic organic compound that consists of a furan ring with a single iodine atom attached to it. 2-Iodofuran is commonly used as a building block in organic synthesis, particularly in the pharmaceutical industry. The iodine atom in the structure of 2-Iodofuran makes it a valuable reagent for various chemical reactions such as substitution, coupling, and metal-catalyzed processes. It is also known for its potential use in the development of new pharmaceuticals and agrochemicals due to its unique structure and reactivity. Additionally, 2-Iodofuran is a useful reagent in the field of organic chemistry and is of interest to researchers and professionals working in medicinal chemistry and material science.
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 articles and documents
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.
