756-76-3 Usage
Uses
Used in Coatings Industry:
Trichloro[3-(1,1,2,2-tetrafluoroethoxy)propyl]silane is utilized as a performance enhancer in the coatings industry, where it is employed to improve the durability and water, oil, and stain resistance of coatings. Its hydrophobic and oleophobic properties are particularly beneficial for applications requiring easy cleaning and maintenance.
Used in Adhesives Industry:
In the adhesives industry, trichloro[3-(1,1,2,2-tetrafluoroethoxy)propyl]silane serves as an adhesion promoter, enhancing the bonding strength between different materials. Its ability to form strong chemical bonds with surfaces contributes to the improved performance and reliability of adhesive products.
Used in Sealants Industry:
Trichloro[3-(1,1,2,2-tetrafluoroethoxy)propyl]silane is used as a key component in sealant formulations to boost their sealing capabilities. trichloro[3-(1,1,2,2-tetrafluoroethoxy)propyl]silane's adherence properties ensure a tight seal, making it ideal for applications in construction, automotive, and aerospace industries where sealing performance is critical.
It is crucial to handle trichloro[3-(1,1,2,2-tetrafluoroethoxy)propyl]silane with appropriate safety measures due to its toxic nature and potential to cause skin, eye, and respiratory irritation. Proper handling and storage protocols are essential to ensure the safety of workers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 756-76-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 756-76:
(5*7)+(4*5)+(3*6)+(2*7)+(1*6)=93
93 % 10 = 3
So 756-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H7Cl3F4OSi/c6-14(7,8)3-1-2-13-5(11,12)4(9)10/h4H,1-3H2
756-76-3Relevant academic research and scientific papers
Process for preparing fluoroalkyl-containing organosilicon compounds, and their use
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, (2008/06/13)
Fluoroalkyl organosilicon compounds are prepared by reacting fluoroolefins with organosilicon compounds that contain at least one H--Si group, in the presence of a Pt(0) complex catalyst. Further, fluoroalkylalkoxy organosilicon compounds are prepared by esterifying fluoroalkyl organosilicon compounds. The process proceeds uniformly under mild conditions with high yields and selectivities.
