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HSiCl2-p-CH3C6H4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13272-80-5

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13272-80-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13272-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,7 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13272-80:
(7*1)+(6*3)+(5*2)+(4*7)+(3*2)+(2*8)+(1*0)=85
85 % 10 = 5
So 13272-80-5 is a valid CAS Registry Number.

13272-80-5Upstream product

13272-80-5Downstream Products

13272-80-5Relevant academic research and scientific papers

SYNTHESIS OF ORGANO CHLOROSILANES FROM ORGANOSILANES

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Page/Page column 36; 37; 38; 39, (2019/04/16)

The invention relates to a process for the production of chlorosilanes by subjecting one or more hydndosilanes to the reaction with hydrogen chloride in the presence of at least one ether compound, and a process for the production of such hydndosilanes serving as starting materials.

Lewis Base Catalyzed Selective Chlorination of Monosilanes

Sturm, Alexander G.,Schweizer, Julia I.,Meyer, Lioba,Santowski, Tobias,Auner, Norbert,Holthausen, Max C.

supporting information, p. 17796 - 17801 (2018/11/23)

A preparatively facile, highly selective synthesis of bifunctional monosilanes R2SiHCl, RSiHCl2 and RSiH2Cl is reported. By chlorination of R2SiH2 and RSiH3 with concentrated HCl/ether solutions, the stepwise introduction of Si?Cl bonds is readily controlled by temperature and reaction time for a broad range of substrates. In a combined experimental and computational study, we establish a new mode of Si?H bond activation assisted by Lewis bases such as ethers, amines, phosphines, and chloride ions. Elucidation of the underlying reaction mechanisms shows that alcohol assistance through hydrogen-bond networks is equally efficient and selective. Remarkably, formation of alkoxysilanes or siloxanes is not observed under moderate reaction conditions.

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