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phenylmethoxydichlorosilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50971-88-5

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50971-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50971-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,7 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50971-88:
(7*5)+(6*0)+(5*9)+(4*7)+(3*1)+(2*8)+(1*8)=135
135 % 10 = 5
So 50971-88-5 is a valid CAS Registry Number.

50971-88-5Relevant academic research and scientific papers

Asymmetric Synthesis of Silicon-Stereogenic Silanes by Copper-Catalyzed Desymmetrizing Protoboration of Vinylsilanes

Li, Yanfei,Wang, Ying,Xiong, Tao,Zhang, Ge,Zhang, Qian

supporting information, p. 11927 - 11931 (2020/05/22)

The catalytic asymmetric creation of silanes with silicon stereocenters is a long-sought but underdeveloped topic, and only a handful of examples have been reported. Moreover, the construction of chiral silanes containing (more than) two stereocenters is a more arduous task and remains unexploited. We herein report an unprecedented copper-catalyzed desymmetrizing protoboration of divinyl-substituted silanes with bis(pinacolato)diboron (B2pin2). This method enables the facile preparation of an array of enantiomerically enriched boronate-substituted organosilanes bearing contiguous silicon and carbon stereocenters with exclusive regioselectivity and generally excellent diastereo- and enantioselectivity.

Convenient synthesis of alkoxyhalosilanes from hydrosilanes

Ohshita, Joji,Taketsugu, Ryosuke,Nakahara, Yuki,Kunai, Atsutaka

, p. 3258 - 3264 (2007/10/03)

Selective dehydrogenative coupling of di- and trihydrosilanes with alcohols catalyzed by PdCl2 or NiCl2 afforded alkoxyhydro- and dialkoxyhydrosilanes in good yield. Further treatment of the resulting alkoxyhydrosilanes with carbon tetrachloride or allyl bromide in the presence of the same catalyst led to the formation of alkoxychloro- and alkoxybromosilanes, respectively. Similar reactions of dialkoxyhydrosilanes with carbon tetrachloride afforded dialkoxychlorosilanes in good yield, although contamination of small amounts of trialkoxysilanes and alkoxydichlorosilanes was detected in the products. Selective substitution of the alkoxyhalosilanes with nucleophiles is also reported.

Reaction of Tetraalkoxysilanes with Alkyl(aryl)chlorosilanes

Chernyshev, E. A.,Komalenkova, N. G.,Tagachenkov, A. A.,Bykovchenko, V. G.

, p. 241 - 243 (2007/10/03)

Alkyl(aryl)trichloro- or dialkyl(diaryl)dichlorosilanes react with tetraalkoxysilanes Si(OMe)4, Si(OEt)4, and Si(OBu)4 to give partially etherfied alkyl(aryl)chlorosilanes RSiCl2(OAlk), RSiCl(OAlk)2, and R2SiCl(OAlk).

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