35569-06-3 Usage
Uses
Used in Plastics Industry:
Dicyclohexyldimethyltin is used as a heat stabilizer for polyvinyl chloride (PVC) to prevent thermal degradation and improve the material's fire resistance. This application is crucial in ensuring the durability and safety of PVC products.
Used in Chemical Synthesis:
In the chemical synthesis industry, dicyclohexyldimethyltin serves as a catalyst in the production of silicone rubber, contributing to the development of high-quality and versatile materials with a wide range of applications.
Used in Organic Chemistry:
Dicyclohexyldimethyltin is utilized as a reactive intermediate in organic chemistry, facilitating various chemical reactions and contributing to the synthesis of complex organic compounds.
However, it is important to note that dicyclohexyldimethyltin poses potential health hazards. It is considered toxic to aquatic life and can cause skin and eye irritation in humans. Therefore, it is crucial to handle this chemical with caution and adhere to safety guidelines to minimize associated risks.
Check Digit Verification of cas no
The CAS Registry Mumber 35569-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,6 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35569-06:
(7*3)+(6*5)+(5*5)+(4*6)+(3*9)+(2*0)+(1*6)=133
133 % 10 = 3
So 35569-06-3 is a valid CAS Registry Number.
InChI:InChI=1/2C6H11.2CH3.Sn/c2*1-2-4-6-5-3-1;;;/h2*1H,2-6H2;2*1H3;/rC14H28Sn/c1-15(2,13-9-5-3-6-10-13)14-11-7-4-8-12-14/h13-14H,3-12H2,1-2H3
35569-06-3Relevant articles and documents
Surface organometallic chemistry on metals: Controlled hydrogenolysis of Me4Sn, Me3SnR, Me2SnR2, MeSnBu 3 and SnBu4 (R = methyl, n-butyl, tert-butyl, neopentyl, cyclohexyl) onto metallic rhodium supported on silica
Taoufik, Mostafa,Cordonnier, Marie-Anne,Santini, Catherine C.,Basset, Jean-Marie,Candy, Jean-Pierre
, p. 1531 - 1537 (2007/10/03)
The controlled hydrogenolysis of MexSnR4-x (0 ≤ x ≤ 4; R = methyl, n-butyl, tert-butyl, neopentyl, cyclohexyl) onto Rh/SiO 2 is followed by quantitative and qualitative analysis of evolved gases. Only MeH and RH are detected in the evolved gases. There is hydrogenolysis of the Sn-C bonds without any C-C bond hydrogenolysis, leading to formation of grafted organometallic fragments. Using various organotin compounds, MexSnR4-x, it has been possible to determine the regioselectivity of the hydrogenolysis of the Sn-C bonds. The initial selectivity is inversely proportional to the steric bulk of the alkyl group: tBu xR4-x (symmetry D3h), in which the bulkiest group, e.g., R, is away from the surface could explain these results. This surface five-coordinate tin species could eliminate an alkyl group, generally a methyl group, thus decreasing the steric bulk around the tin, into the equatorial plane of D3h, via a concerted hydrogen transfer-elimination mechanism to give Rh-SnMex-1R4-x. Then, in the successive steps of the hydrogenolysis, the bulkiest group, R, would be eliminated.
