17306-05-7 Usage
General Description
Phenylmethylvinylchlorosilane is an organosilicon compound with the chemical formula C10H13ClSi. It is commonly used as a precursor in the production of various silicon-based materials and compounds. Phenylmethylvinylchlorosilane is a colorless liquid with a pungent odor and it is highly reactive with water and air. It is commonly employed in the manufacturing of silicone polymers, resins, and adhesives, as a coupling agent in rubber and plastic compounds, and as a surface modifier in coatings and sealants. PHENYLMETHYLVINYLCHLOROSILANE is also used as a reagent in organic synthesis and as a crosslinking agent in the production of elastomers and copolymers. It is important to handle phenylmethylvinylchlorosilane with caution due to its flammability and reactivity with water and air.
Check Digit Verification of cas no
The CAS Registry Mumber 17306-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,0 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17306-05:
(7*1)+(6*7)+(5*3)+(4*0)+(3*6)+(2*0)+(1*5)=87
87 % 10 = 7
So 17306-05-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H11ClSi/c1-3-11(2,10)9-7-5-4-6-8-9/h3-8H,1H2,2H3
17306-05-7Relevant articles and documents
Synthesis of difunctional 1,4-dimethyl-1,4-disilacyclohexanes
Volkova,Petrova,Chizhova,Petrovskii,Vinogradova,Makarova
, p. 1712 - 1716 (2007/10/03)
Transformations of HVinSiCl2, HVinSi(Me)Cl, HVinSi(Me)Ph, and HVinSi(Me)NEt2 in the presence of Pt catalyst were studied. In dilute solutions, the reaction gave a mixture of structural and stereoisomers of five- and six-membered disilacyclanes, resulting from intramolecular cyclization of the initially formed linear dimer. In the case of methyl(phenyl)disilacyclane, the structural isomers were separated and tran.s-1,4-dimethyl-1,4-diphenyl-1,4-disilacyclohexane was isolated. The reaction of this product with HCI in the presence of AlCl3 followed by hydrolysis resulted in the synthesis of trans-1,4-dichloro- and trans-1,4-dihydroxy-1,4-dimethyl-1,4-disilacyclohexanes. The structures of the structural and stereoisomers synthesized were confirmed by 1H, 13C, and 29Si NMR and IR spectroscopies and mass spectrometry.
