70851-47-7 Usage
Uses
Used in Silicone Rubber Production:
CHLOROMETHYLDODECYLDIMETHYLSILANE is used as a surface modifying agent in the production of silicone rubber, enhancing the material's properties and performance.
Used in Synthesis of Organic and Inorganic Materials:
As a coupling agent, CHLOROMETHYLDODECYLDIMETHYLSILANE is utilized in the synthesis of various organic and inorganic materials, improving their adhesion and compatibility.
Used in Adhesives Industry:
CHLOROMETHYLDODECYLDIMETHYLSILANE is used as a component in adhesive formulations, providing strong bonding capabilities due to its reactive nature and covalent bonding potential.
Used in Coatings Industry:
In the coatings industry, CHLOROMETHYLDODECYLDIMETHYLSILANE is employed to improve the adhesion, durability, and water resistance of coatings.
Used in Sealants Industry:
CHLOROMETHYLDODECYLDIMETHYLSILANE is used in sealant formulations to enhance their sealing properties and resistance to environmental factors.
Used in Personal Care and Cosmetic Products:
CHLOROMETHYLDODECYLDIMETHYLSILANE is used as a surfactant or dispersing agent in the formulation of personal care and cosmetic products, leveraging its hydrophobic and lipophilic properties to improve product performance and stability.
Check Digit Verification of cas no
The CAS Registry Mumber 70851-47-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,5 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70851-47:
(7*7)+(6*0)+(5*8)+(4*5)+(3*1)+(2*4)+(1*7)=127
127 % 10 = 7
So 70851-47-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H33ClSi/c1-4-5-6-7-8-9-10-11-12-13-14-17(2,3)15-16/h4-15H2,1-3H3
70851-47-7Relevant academic research and scientific papers
Cross-linked heparin coatings and methods
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, (2009/01/24)
A thromboresistant coating for a medical device, method of coating and coated medical device, the coating including an in situ cross-linked co-polymer of a cross-linkable biomolecule, preferably an adsorbable biomolecule such as a heparin activity biomolecule with at least one prosthetic hydrophobic unit, and a multifunctional crosslinking agent, such as a bis-variant of polyethylene glycol, polyethylene oxide, or polyethylene glycol, wherein the crosslinking is by means of covalent complexation through at least two functional groups of the multifunctional crosslinking agent.
Process for the preparation of lactic acid silyl esters
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, (2008/06/13)
Novel lactic acid silyl esters of the formula STR1 in which R represents alkyl or aryl, are obtained by a new process which comprises reacting a lactic acid of the formula STR2 with a chloromethylsilane of the formula STR3 in which R has the meaning indicated above, in the presence of a tertiary amine and, if appropriate, in the presence of an additional diluent, at temperatures between 50° and 120° C.
