22214-92-2 Usage
Uses
Used in Pharmaceutical Industry:
(1Z)-1-ethyl-2-iodobut-1-en-1-yl 4-methylphenyl sulfone is used as a synthetic intermediate for the development of pharmaceuticals. Its reactivity and versatility in chemical reactions allow for the creation of various drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, (1Z)-1-ethyl-2-iodobut-1-en-1-yl 4-methylphenyl sulfone is utilized as a building block for the synthesis of agrochemicals. Its unique structure and functional groups contribute to the development of new compounds with pesticidal or herbicidal properties.
Used in Organic Synthesis:
(1Z)-1-ethyl-2-iodobut-1-en-1-yl 4-methylphenyl sulfone serves as a key component in organic synthesis, where its iodine and sulfone groups can participate in various reactions. This makes it a valuable precursor for the synthesis of complex organic molecules and specialty chemicals.
It is crucial to handle and use (1Z)-1-ethyl-2-iodobut-1-en-1-yl 4-methylphenyl sulfone with care due to the potentially hazardous nature of its 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 academic research and scientific papers
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.
