467426-68-2 Usage
General Description
(cis)-N,N-diethyl-2-iodocyclopropanecarboxamide, also known as iodozide, is a chemical compound that belongs to the class of carboxamides. It is characterized by a cyclopropane ring structure with a carboxamide group and an attached iodine atom. (cis)-N,N-diethyl-2-iodocyclopropanecarboxaMide is primarily used as a reagent in organic synthesis, particularly in the preparation of various biologically active compounds and pharmaceuticals. Its unique structure and reactivity make it a valuable tool in the development of new molecules for medicinal and research purposes. Additionally, it has also been studied for its potential applications in materials science and other fields of chemistry. However, it should be handled with caution due to its potentially hazardous properties.
Check Digit Verification of cas no
The CAS Registry Mumber 467426-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,7,4,2 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 467426-68:
(8*4)+(7*6)+(6*7)+(5*4)+(4*2)+(3*6)+(2*6)+(1*8)=182
182 % 10 = 2
So 467426-68-2 is a valid CAS Registry Number.
467426-68-2Relevant articles and documents
Total Synthesis of Cardiolipins Containing Chiral Cyclopropane Fatty Acids
Inuki, Shinsuke,Ohta, Ippei,Ishibashi, Shunichi,Takamatsu, Masayuki,Fukase, Koichi,Fujimoto, Yukari
, p. 7832 - 7838 (2017/08/14)
Cardiolipin (CL) is a phospholipid located in both the eukaryotic mitochondrial inner membrane and the bacterial cell membrane. Some bacterial CLs are known to contain cyclopropane moieties in their acyl chains. Although the CLs are thought to be involved in the innate immune response, there have been few attempts at chemical synthesis of the CLs, and detailed studies of their biological activities are scarce. Thus, we have developed a synthetic route to CLs containing chiral cyclopropane moieties.
BuMgNiPr2: A new base for stoichiometric, position-selective deprotonation of cyclopropane carboxamides and other weak CH acids
Zhang, Mao-Xi,Eaton, Philip E.
, p. 2169 - 2171 (2007/10/03)
Using the irreversible formation of an alkane, the proton-removing ability of a magnesiated amine, and the activating effect of a carboxamido group, weakly acidic CH groups E in a variety of systems can be selectively converted into useful amido-Grignard
