166970-54-3 Usage
Uses
Used in Chemical Synthesis:
Allyl(chloropropyl)dichlorosilane is used as a precursor in the synthesis of various organosilicon compounds, such as silicones and silanes, due to its reactive nature and ability to form stable siloxane bonds.
Used in Specialty Polymers and Coatings:
In the polymer industry, Allyl(chloropropyl)dichlorosilane is used as a crosslinking agent to enhance the mechanical properties, thermal stability, and chemical resistance of specialty polymers and coatings.
Used in Adhesives and Sealants:
Allyl(chloropropyl)dichlorosilane is employed as a reactive component in the formulation of high-performance adhesives and sealants, providing improved adhesion, flexibility, and durability.
Used in Electronic Materials:
In the electronics industry, Allyl(chloropropyl)dichlorosilane is utilized in the development of encapsulants and potting compounds for electronic devices, offering excellent electrical insulation and thermal conductivity.
Used in Textile Industry:
Allyl(chloropropyl)dichlorosilane is used as a finishing agent in the textile industry to impart water-repellent, soil-release, and anti-static properties to fabrics.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care industry, Allyl(chloropropyl)dichlorosilane is used as a conditioning agent, providing smoothness, softness, and manageability to hair and skin care products.
Used in Laboratory Research:
Allyl(chloropropyl)dichlorosilane is employed as a reagent in various laboratory research applications, including the study of organosilicon chemistry, polymer synthesis, and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 166970-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,9,7 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 166970-54:
(8*1)+(7*6)+(6*6)+(5*9)+(4*7)+(3*0)+(2*5)+(1*4)=173
173 % 10 = 3
So 166970-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H11Cl3Si/c1-2-5-10(8,9)6-3-4-7/h2H,1,3-6H2
166970-54-3Relevant academic research and scientific papers
Mansel, Stefan,Rief, Ursula,Prosenc, Marc-Heinrich,Kirsten, Robin,Brintzinger, Hans-Herbert
, p. 225 - 236 (1996)
Chiral ansa-zirconocene complexes with a trimethylene link between the Si bridge atom and an α-position of each C5 ring ligand were prepared; two representatives, with i-propyl and t-butyl groups as β-substituents, were structurally characterized. The properties of these complexes with respect to MAO-activated propene polymerization were studied in comparison with those of their Me2Si-bridged analogs. The t-butyl-substituted spirosilane complex gives a polymer with relatively high content of 3,1-insertions. These increased regioirregularities appear to be associated with decreased coordination gap aperture and increased lateral extension angles of the spirosilane-bridged zirconocene complexes; this notion is supported by a molecular-mechanics analysis of alternative olefin-insertion transition states.
Allylalkylsilanes and their preparation methods
-
, (2008/06/13)
The present invention relates to allylakylsilanes represented by the general formula (III) and their preparation methods by reacting allylsilanes represented by the formula I with olefin compounds represented by the formula II in the presence of hydrosilation catalysts such as chloroplatinic acid, platinum on silica, tributyl amine and Pd, Rh, Ni metals. STR1 wherein X represents independently chloro or alkoxy (C1-C4) and R is selected from the group consisting of Ph, CH2 Cl, Cn H2n CH3 (n=0-15), Si(Me)m Cl3-m (m=0-3), CF3, CH2 CF3, CN, CH2 CN, STR2 CH2 Si(Me)m CL3-m (m=0-3), Si(Me)m (OR1)3-m (m=0-3), CH2 Si(Me)m (OR1)3-m (m=0-3), (wherein Me is methyl and R1 is methoxy or ethoxy group), Ph-CH2 Cl, and cyclohexenyl group.
