5833-60-3 Usage
Uses
Used in Organosilicon Chemistry:
2,2,6,6-tetramethyl-1,4,2,6-dioxadisilinane is used as a precursor in the synthesis of other organosilicon compounds. Its cyclic structure and reactivity make it a valuable intermediate for the preparation of a wide range of organosilicon materials.
Used in Silicone Polymers and Elastomers Production:
2,2,6,6-tetramethyl-1,4,2,6-dioxadisilinane is used as a cross-linking agent in the production of silicone polymers and elastomers. Its ability to form stable linkages between polymer chains contributes to the enhanced mechanical properties and thermal stability of the final products.
Used in Polysiloxane Manufacture:
2,2,6,6-tetramethyl-1,4,2,6-dioxadisilinane is utilized as a co-catalyst in the manufacture of polysiloxanes. Its catalytic activity aids in the efficient synthesis of polysiloxanes, which are essential components in various silicone-based products.
Used in Silicone Resins Production:
2,2,6,6-tetramethyl-1,4,2,6-dioxadisilinane is employed in the production of silicone resins. Its presence in the resin formulation helps to improve the resin's properties, such as adhesion, flexibility, and resistance to environmental factors.
Check Digit Verification of cas no
The CAS Registry Mumber 5833-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5833-60:
(6*5)+(5*8)+(4*3)+(3*3)+(2*6)+(1*0)=103
103 % 10 = 3
So 5833-60-3 is a valid CAS Registry Number.
5833-60-3Relevant academic research and scientific papers
Phosphorus-containing disiloxanes: Synthesis and thermal rearrangement of the 1,2-shift type
Molchanova,Shcherbina,Petrovskii,Nifant'ev
, p. 1245 - 1249 (2007/10/03)
Methods for the synthesis of tetramethylbis(ω-phosphoryloxyalkyl) disiloxanes were developed. Thermal rearrangement of the 1,2-shift type of tetramethylbis(phosphoryloxymethyl)disiloxanes was studied. The 1,2-shift rearrangement of dimethyl(diphenoxyphosp
