2943-86-4 Usage
Description
Triethyliodotin(IV), with the molecular formula C6H15ISn and a molar mass of approximately 345.80 g/mol, is a chemical compound consisting of three ethyl groups and one iodine atom bonded to a tin atom. It is typically a white crystalline solid with a melting point of around 120-125 degrees Celsius. Known for its catalytic properties in organic synthesis reactions, Triethyliodotin(IV) plays a significant role in the chemical industry.
Uses
Used in Organic Synthesis:
Triethyliodotin(IV) is used as a catalyst in organic synthesis reactions for its ability to facilitate various chemical transformations, enhancing the efficiency and selectivity of the processes.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Triethyliodotin(IV) is utilized as a catalyst in the synthesis of various drugs, contributing to the development of new medications and improving the manufacturing processes.
Used in Plastics Industry:
Triethyliodotin(IV) is employed in the production of plastics, where it acts as a catalyst to speed up the polymerization reactions, resulting in the formation of desired plastic materials with specific properties.
Used in Other Industrial Materials:
Beyond pharmaceuticals and plastics, Triethyliodotin(IV) finds applications in the production of other industrial materials, where its catalytic properties are harnessed to improve the synthesis and properties of these materials.
Check Digit Verification of cas no
The CAS Registry Mumber 2943-86-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2943-86:
(6*2)+(5*9)+(4*4)+(3*3)+(2*8)+(1*6)=104
104 % 10 = 4
So 2943-86-4 is a valid CAS Registry Number.
InChI:InChI=1/3C2H5.HI.Sn/c3*1-2;;/h3*1H2,2H3;1H;/q;;;;+1/p-1/rC6H15ISn/c1-4-8(7,5-2)6-3/h4-6H2,1-3H3
2943-86-4Relevant articles and documents
Lorberth, J.,Vahrenkamp, H.
, p. 111 - 124 (1968)
Reactions of (triethylstannylthioalkyl)trialkoxysilanes and (triethylstannylthioalkyl)trialkoxysilatranes with methyl iodide
Sorokin,Voronkov
experimental part, p. 2056 - 2060 (2009/04/13)
Reactions of (triethylstannylthioalkyl)trimethoxysilanes Et 3SnS(CH2)nSi(OMe)3 (n = 1, 2) and (triethylstannylthioalkyl)trialkoxysilatranes Et3Sn(CH2) n Sa [hereinafter Sa = Si(O
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.
