22214-92-2 Usage
General Description
"(1Z)-1-ethyl-2-iodobut-1-en-1-yl 4-methylphenyl sulfone" is a chemical compound that contains an iodine and a sulfur component. The structure of the compound consists of an ethyl group attached to a butenyl group with an iodine atom, and a 4-methylphenyl sulfone group. It is a potentially important chemical in organic synthesis due to the presence of the iodine and sulfone functional groups, which can participate in various reactions such as substitution, oxidation, and elimination. The compound may have potential applications in pharmaceuticals, agrochemicals, and other industries due to its reactivity and versatility in chemical reactions. However, it is important to handle and use this compound with caution due to the potentially hazardous constituents.
Check Digit Verification of cas no
The CAS Registry Mumber 22214-92-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,1 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22214-92:
(7*2)+(6*2)+(5*2)+(4*1)+(3*4)+(2*9)+(1*2)=72
72 % 10 = 2
So 22214-92-2 is a valid CAS Registry Number.
22214-92-2Relevant articles and documents
Stereoselective Bifunctionalization of Alkynes by Means of the Mercury(II) Salt-Iodine Combination
Barluenga, Jose,Martinez-Gallo, Jose M.,Najera, Carmen,Yus, Miguel
, p. 1017 - 1020 (2007/10/02)
The reaction of alkynes with iodine and mercury(II) salts (chloride, acetate, methanesulphonate, toluene-p-sulphonate, benzylsulphide, toluene-p-sulphinate, and thiocyanate) affords stereoselectively E-β-functionalized vinyl iodides resulting from the ionic addition of iodine and the mercury(II) salt anion.Unsymmetrical alkynes yield regiospecifically Markovnikov addition products.In the case of mercury(II) thiocyanate the reaction can be used also for the stereoselective preparation of E-1,2-dithiocyanatoalkenes.An ionic mechanism is proposed according to the observed regio- and stereochemistry.
