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1,2-Di(silyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63128-20-1

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63128-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63128-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,2 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63128-20:
(7*6)+(6*3)+(5*1)+(4*2)+(3*8)+(2*2)+(1*0)=101
101 % 10 = 1
So 63128-20-1 is a valid CAS Registry Number.

63128-20-1Relevant academic research and scientific papers

Synthesis, Structural Characterization and Reactivity of a Bis(phosphine)(silyl) Platinum(II) Complex

Li, Yonghua,Zeng, Wenjin,Lai, Wenyong,Shimada, Shigeru,Wang, Shi,Wang, Lianhui,Huang, Wei

, p. 1206 - 1210 (2015)

Treatment of 1,2-C6H4(SiH3)(SiH3) (1) with Pt(dmpe)(PEt3)2 (dmpe=Me2PCH2CH2PMe2) in the ratio of 1:1 leads to the complex {1,2-C6Hsub

Synthesis, structural characterization and reactivity towards methanol of a bis(silyl)platinum(II) complex bearing a chelating depe ligand

Zeng, Wen-Jin,Guo, Jin-Fei,Sun, Shuang-Shuang,Li, Yong-Hua,Zhu, Jia-Yi,Huang, Chao,Wang, Shi,Huang, Wei

, p. 93 - 96 (2016)

Treatment of 1,2-C6H4(SiH3)(SiH3) (1) with [Pt(depe)(PEt3)2] (depe = Et2PCH2CH2PEt2) in the ratio of 1:1 yields the complex [PtII{1,2-

Synthesis, structural characterization and reactivity of a bis(phosphine)(silyl) platinum(II) complex

Li, Yong-Hua,Yang, Cheng-Long,Lai, Wen-Yong,Huang, Zheng-Feng,Wang, Shi,Wang, Lian-Hui,Huang, Wei

, p. 181 - 184 (2015)

Treatment of 1,2-C6H4(SiH3)(SiH3) (1) with Pt(dcpe)(PEt3)2 (dcpe = Cy2PCH2CH2PCy2) in dry toluene at room temperature in the ratio of 1:1 leads t

1,2-Di(silyl)benzene and 1,4-Dibromo-2,5-di(silyl)benzene

Schroeck, Robert,Sladek, Alexander,Schmidbaur, Hubert

, p. 1036 - 1040 (2007/10/02)

1,2-Di(silyl)benzene (3), has been prepared in a three-step process starting with the reaction of 1,2-dibromobenzene and p-tolyl(chloro)silane with magnesium in tetrahydrofuran, which affords 1,2-bis(p-tolylsilyl)benzene (1) as a stable high-yield intermediate.Compound 1 has been converted into 1,2-bis(trifluoromethanesulfonatosilyl)benzene (2) with trifluoromethanesulfonic acid, and finally into 3 by reduction with lithiumaluminiumhydride, both again in high yields. - In an attempt to prepare 1,2,4,5-tetra(silyl)benzene in an analogous way, only the bis-silylated species could be obtained (from 1,2,4,5-C6H2Br4, p-MeC6H4SiClH2 and Mg powder: 1,4-dibromo-2,5-bis(p-tolylsilyl)benzene, 4, and 1,4-dibromo-2,5-di(silyl)benzene, 6, via 1,4-dibromo-2,5-bis(trifluoromethanesulfonatosilyl)benzene, 5).The crystal structures of compounds 4 and 6 have been determined by X-ray diffraction.The results indicate no steric hindrance in these molecules and it is thus not obvious from the molecular structures why the silylation reaction does not proceed any further to give the tetrasilylated benzene derivatives.Electronic effects have to be invoked to rationalize the experimental findings. - Keywords: Silanes, Silylbenzenes, Di(silyl)benzenes, Bromo(silyl)benzenes

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