26037-72-9 Usage
Uses
Used in Organic Synthesis:
Iodo(p-tolyl)mercury(II) is utilized as a reagent for the introduction of mercury and iodine into organic molecules. Its ability to facilitate the incorporation of these elements into complex organic structures makes it a valuable tool in the synthesis of various organic compounds.
Used in Catalysis:
In the field of catalysis, Iodo(p-tolyl)mercury(II) serves as a catalyst in certain chemical reactions. Its catalytic properties can enhance the efficiency and selectivity of specific chemical processes, contributing to the advancement of chemical research and industrial applications.
Used in Research:
Due to its unique properties and reactivity, Iodo(p-tolyl)mercury(II) is also employed in research settings to explore new chemical reactions and mechanisms, further expanding the understanding of mercury and iodine chemistry.
It is crucial to handle Iodo(p-tolyl)mercury(II) with caution due to its toxic nature, which can pose risks to human health and the environment if mismanaged. Proper safety measures and disposal methods must be strictly adhered to when working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 26037-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,3 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26037-72:
(7*2)+(6*6)+(5*0)+(4*3)+(3*7)+(2*7)+(1*2)=99
99 % 10 = 9
So 26037-72-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H7.Hg.HI/c1-7-5-3-2-4-6-7;;/h3-6H,1H3;;1H/q;+1;/p-1/rC7H7HgI/c1-6-2-4-7(8-9)5-3-6/h2-5H,1H3
26037-72-9Relevant articles and documents
Substituent effects in aromatic substitution of aryltriethyltin compounds by mercuric halides
Sedaghat-Herati, M. Reza,Sharifi, Taghi
, p. 39 - 44 (2007/10/02)
Second-order rate constants are reported for the reaction of some YC6H4SnEt3 compounds with mercuric halides in tetrahydrofuran, and show that the reaction is one of low selectivity.The substituent effects can be correlated only in terms of Hammett ?-constants, and the data for the meta-methoxy group are anomalous.The results indicate that the rate determining step involves reaction of a ?-complex.Activation parameters are reported, and are in accordance with the suggested mechanism.
