17886-88-3 Usage
General Description
4-Phenylbutyltrichlorosilane is an organosilicon compound primarily used as a coupling agent in the production of silane-modified polymers and organic surface modification. It is also used as a potential intermediate in the synthesis of pharmaceuticals and other organic compounds. The chemical structure of 4-phenylbutyltrichlorosilane consists of a trichlorosilane group attached to a four-carbon alkyl chain with a phenyl group attached to the third carbon atom. 4-PHENYLBUTYLTRICHLOROSILANE can react with various organic and inorganic substrates to form strong covalent bonds, making it valuable as a functionalizing agent for a variety of applications in the chemical and pharmaceutical industries. However, its handling and use require appropriate safety precautions due to its corrosive and potentially hazardous nature.
Check Digit Verification of cas no
The CAS Registry Mumber 17886-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,8 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17886-88:
(7*1)+(6*7)+(5*8)+(4*8)+(3*6)+(2*8)+(1*8)=163
163 % 10 = 3
So 17886-88-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H13Cl3Si/c11-14(12,13)9-5-4-8-10-6-2-1-3-7-10/h1-3,6-7H,4-5,8-9H2
17886-88-3Relevant articles and documents
Radical addition of silanes to alkenes followed by oxidation
Palframan, Matthew J.,Parsons, Andrew F.,Johnson, Paul
experimental part, p. 2811 - 2814 (2012/01/06)
Phenyldimethylsilane and trichlorosilane are shown to undergo efficient radical hydrosilylation reactions, on reaction with various alkenes, using triethylborane as the initiator. Adducts from the trichlorosilane reactions can be oxidised to afford alcohols in good yields. This two-step process leads to the anti-Markovnikov hydration of alkenes. Georg Thieme Verlag Stuttgart · New York.
Catalytic Asymmetric Synthesis of Optically Active 2-Alkanols via Hydrosilylation of 1-Alkenes with a Chiral Monophosphine-Palladium Catalyst
Uozumi, Yasuhiro,Hayashi, Tamio
, p. 9887 - 9888 (2007/10/02)
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