13302-06-2 Usage
Uses
Used in Organic Synthesis:
Tributylstannyl methanesulfonate is used as a reagent for facilitating carbon-carbon bond formation in organic synthesis. Its unique properties make it a valuable tool in creating complex organic molecules and structures.
Used in Organotin Chemistry:
In the field of organotin chemistry, tributylstannyl methanesulfonate is employed as a key component in various reactions. Its presence can enhance the reactivity and selectivity of organotin compounds, contributing to the advancement of organotin chemistry.
Used in Coupling Reactions:
Tributylstannyl methanesulfonate is utilized as a coupling agent in chemical reactions. It aids in the joining of different molecular fragments, which is crucial for the synthesis of a wide range of organic compounds.
If there are specific industries where tributylstannyl methanesulfonate is applied differently, they can be listed as follows:
Used in Pharmaceutical Industry:
Tributylstannyl methanesulfonate is used as a synthetic intermediate for the development of pharmaceutical compounds. Its ability to form carbon-carbon bonds is essential in the creation of complex drug molecules.
Used in Material Science:
In material science, tributylstannyl methanesulfonate is used as a precursor in the synthesis of organotin polymers and materials. These materials have potential applications in various areas, including as catalysts, stabilizers, or components of advanced materials with unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 13302-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,0 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13302-06:
(7*1)+(6*3)+(5*3)+(4*0)+(3*2)+(2*0)+(1*6)=52
52 % 10 = 2
So 13302-06-2 is a valid CAS Registry Number.
InChI:InChI=1/3C4H9.CH4O3S.Sn/c3*1-3-4-2;1-5(2,3)4;/h3*1,3-4H2,2H3;1H3,(H,2,3,4);/rC12H27Sn.CH4O3S/c1-4-7-10-13(11-8-5-2)12-9-6-3;1-5(2,3)4/h4-12H2,1-3H3;1H3,(H,2,3,4)
13302-06-2Relevant academic research and scientific papers
Farah, Dan,Swami, Kamal,Kuivila, Henry G.
, p. 311 - 334 (1992)
A study of the syntheses and some properties of several methyl substituted acyclic and cyclic bidentate organotin Lewis acids has been carried out.Of particular interest were cyclic species with 7-, 8-, 9- and 10-membered rings.The distannalkanes and distannacycloalkanes were converted to the chlorides by chlorodemethylation with tin chlorides or mercuric chloride; this reaction was accompanied by ring cleavage in some cases.Chlorides, in turn, were readily converted to the methanesulfonates and trifluoromethanesulfonates. 1H, 13C and 119Sn NMR and IR spectral data were used to gain information concerning structures, conformations and aggregation behavior.The mesylates are associated in chloroform; the triflates are not.
