7719-03-1 Usage
Uses
Used in Organic Synthesis:
ALLYLPHENYLDICHLOROSILANE is used as a reagent in organic synthesis for its high reactivity, which facilitates a wide range of chemical reactions.
Used in Silicon-Based Material Production:
It serves as a precursor in the production of various silicon-based materials, contributing to the development of new materials with unique properties.
Used in Polymer Synthesis:
ALLYLPHENYLDICHLOROSILANE is used as a coupling agent in the synthesis of polymers, enhancing the linkage between different components in the polymer structure.
Used in Specialty Chemicals Manufacturing:
It is utilized in the manufacturing of specialty chemicals, where its unique properties can be leveraged to create high-value products.
Used in the Production of Silicon-Containing Products:
ALLYLPHENYLDICHLOROSILANE is employed in the production of various silicon-containing products, where its reactivity and compatibility with other compounds are advantageous.
Safety Precautions:
Due to its hazardous nature, ALLYLPHENYLDICHLOROSILANE requires proper safety measures during handling and storage to prevent flammable incidents and minimize the risk of skin and eye irritation.
Check Digit Verification of cas no
The CAS Registry Mumber 7719-03-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7719-03:
(6*7)+(5*7)+(4*1)+(3*9)+(2*0)+(1*3)=111
111 % 10 = 1
So 7719-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H10Cl2Si/c1-2-8-12(10,11)9-6-4-3-5-7-9/h2-7H,1,8H2
7719-03-1Relevant academic research and scientific papers
Controlled introduction of allylic group to chlorosilanes
Li, Zhifang,Cao, Xiaojun,Lai, Guoqiao,Liu, Jinhua,Ni, Yong,Wu, Jirong,Qiu, Huayu
, p. 4740 - 4746 (2007/10/03)
Allylation of chlorosilanes has been achieved with allylsamarium bromide, especially in a controlled manner. Thus allylation of trisubstituted chlorosilanes (R3SiCl) afforded a variety of aryl, aralkyl, and alkenyl substituted allylsilanes. Dichlorosilanes (R2SiCl2) can either afford monoallylated silanes or diallylated silanes depending on the amount of allylsamarium bromide used. Similarly, trichlorosilanes (RSiCl3) can selectively afford mono-, di-, and tri-allylation products. Finally, perchlorosilane (SiCl4) was allylated stepwise and the corresponding silanes containing one, two, three or four allylic groups, respectively, were obtained in satisfactory yields.
Macrocyclic polyether compounds
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, (2008/06/13)
Macrocyclic polyether "crown" compounds of the formula EQU1 WHEREIN T is a C2 -C3 alkylene, A is EQU2 R being H or C1 -C18 alkyl, R2 and R3 being independently C1 -C18 alkyl, C2 -C4 alkenyl, or C6 -C14 aryl; Q and Z are independently 1,2-arylene (or saturated derivatives thereof) or substituted 1,2-arylene (or saturated derivatives thereof); a is 0, 1, 2, or 3; b is an integer from 3 to 20; y is 1 or zero; x1, x2, x3, and x4 are integers independently selected to give a 15-60 atom ring. Such crown compounds are generally useful in the formation of complexes with ionic metal compounds, thus making it possible to use certain chemical reagents in media wherein they are normally insoluble.
