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27628-30-4

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27628-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27628-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,2 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27628-30:
(7*2)+(6*7)+(5*6)+(4*2)+(3*8)+(2*3)+(1*0)=124
124 % 10 = 4
So 27628-30-4 is a valid CAS Registry Number.

27628-30-4Relevant academic research and scientific papers

The preparation and crystal structures of the compounds (Ph2MeSi)3CMCl (M=Zn, Cd, or Hg)

Al-Juaid, Salih S.,Eaborn, Colin,Habtemariam, Abraha,Hitchcock, Peter B.,Smith, J. David,et al.

, p. 45 - 56 (1993)

The compounds (PhMe2Si)3CMCl (M=Zn, Cd, or Hg) have been prepared by reaction of (PhMe2Si)3CLi with the chlorides MCl2; for M=Zn or Cd they were obtained via (isolated) Li-containing intermediates thought to .The crystal struc

Comparison of tris(dimethylphenylsilyl)methyllithium and tris(trimethylsilyl)methyllithium reactions with carbon disulfide: A new route for the synthesis of some 1,1-bis(benzylthio) and bis(allylthio)-2,2- bis(dimethylphenylsilyl)ethenes

Safa, Kazem D.,Ghorbanpour, Khatereh

, p. 304 - 311 (2014/04/03)

A series of bis(benzylthio) and bis(allylthio)-2,2-bis(dimethylphenylsilyl) ethenes has been obtained by the reaction of (PhMe2Si) 3CLi and CS2 with benzyl and allyl bromides. A plausible mechanism for the formation of these compounds has been proposed. The reactivity of (PhMe2Si)3CLi toward CS2 has been compared with that of (Me3Si)3CLi. The reaction of (PhMe 2Si)3CLi with CS2 and 2-methyloxirane gave a cyclic thiocarbonate(equation presented). 2014

Synthesis of novel calix[4]arenes containing organosilicon groups

Safa, Kazem D.,Oskoei, Yones Mosaei

scheme or table, p. 26 - 31 (2010/10/01)

Metalation of (RSiMe2)3CH (1a R = H, 1b R = Me, 1c R = Ph) with lithium diisopropylamide (LDA) or methyllithium in THF gave organolithium reagents (RSiMe2)3CLi, which reacted with the formylated calixarene (2),

Some methyl derivatives of phosphorus. The crystal structure of

Al-Juaid, Salih S.,Dhaher, Saadi M.,Eaborn, Colin,Hitchcock, Peter B.,McGeary, Catherine A.,Smith J. David

, p. 39 - 52 (2007/10/02)

The compounds TsiPCl2 (Tsi=(Me3Si)3C) (I), and TpsiPCl2 (Tpsi= (II), have been obtained by the reaction of TsiLi or TpsiLi with PCl3.In the case of TsiLi the reaction conditions could be varied so that 50 percent yields of the diphosphene Tsi

Synthesis and properties of some crowded organotin compounds

Dhaher, Saadi M.,Eaborn, Colin,Smith, J. David

, p. 33 - 44 (2007/10/02)

The preparations of the compounds (Me3Si)3CSnMe2X (X= Cl, Br, I, CN, NCS, O2CMe, O2CCF3, O3SMe, or NO3), (Me3Si)3CSnPh2X (X= Cl or Br), and (Me2PhSi)3CSnMe2X (X= Me, Cl, Br or I) are described.Treatment of (Me2PhSi)3CSnMe2Cl with one equivalent of MeLi gives (Me2PhSi)3CSnMe3, but with additional MeLi (Me2PhSi)3CLi is formed.The compound (Me3Si)2C(SnMe3)2 is obtained by reaction of (Me3Si)2CCl2 with either one or two equivalents of Me3SnLi, and on treatment with MeLi gives the useful reagent (Me3Si)2(Me3Sn)CLi.The latter reacts with Me2SiCl2 and give (Me3Si)2(Me3Sn)C(SiMe2Cl) and with Me2SiHCl to give (Me3Si)2(Me3Sn)C(SiMe2H), which reacts with a one molar proportion of Br2 to give (Me3Si)2(Me3Sn)C(SiMe2Br), and with a two molar proportion of Br2 to give (Me3Si)2C(SnMe2Br)(SiMe2Br).Reaction of (Me3Si)2C(SnMe3)2 with two equivalents of ICl or Br2 gives the dihalides (Me3Si)2C(SnMe2X)2 (X= Cl or Br), and reaction of (Me3Si)2C(SnMe2Br)(SiMe2Br) with PhLi gives (Me3Si)2C(SnMe2Ph)(SiMe2Br).

Reactions at Silicon Centres bearing the Bulky Tris(phenyldimethylsilyl)methyl Ligand

Eaborn, Colin,Mansour, Abdulrahman I.

, p. 729 - 736 (2007/10/02)

Metallation of (PhMe2Si)3CH with MeLi in tetrahydrofuran gives (PhMe2Si)3CLi, which reacts with MeI to give (PhMe2Si)3CMe, and also with Me2SiHCl and MeSiHCl2, to give (PhMe2Si)3CSiMe2H and (PhMe2Si)3CSiMe(H)Cl, respectively, but not with Me3SiCl or a ran

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