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Silane, dichloroethyl(2-phenylethenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90260-89-2

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90260-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90260-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,6 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90260-89:
(7*9)+(6*0)+(5*2)+(4*6)+(3*0)+(2*8)+(1*9)=122
122 % 10 = 2
So 90260-89-2 is a valid CAS Registry Number.

90260-89-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-β-phenyl(ethyldichlorosilyl)ethylene

1.2 Other means of identification

Product number -
Other names trans-Ethyl-dichlor-styryl-silan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:90260-89-2 SDS

90260-89-2Relevant academic research and scientific papers

SILANOL DERIVATIVES AS INHIBITORS OF HISTONE DEACETYLASE

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Page/Page column 89, (2008/06/13)

The present invention is directed to certain silanol derivatives that are inhibitors of histone deacetylase and are therefore useful in the treatment of diseases associated with histone deacetylase activity. Pharmaceutical compositions and processes for p

H2OsCl6 AS CATALYST IN HYDROSILYLATION REACTIONS

Kopylova, L. I.,Lukevits, E.,Voronkov, M. G.

, p. 397 - 402 (2007/10/02)

Hydrosilylation of monosubstituted acetylenes RCCH (R = Bu, Ph) with triethyl-, triethoxy-, dialkylchloro-, or alkyldichlorosilanes, catalyzed by H2OsCl6*6H2O, yields three adducts: internal (α) and two terminal (β) cis and trans stereoisomers, the latter being predominant.Hydrosilylation of ClCH2CCH occurs stereospecifically, giving, along with the prevailing α adduct, trans-β adduct as well.The reactivity of RnSiHX(3-n) in the hydrosilylation decreases in the following order: Me2SiHCl > MeSiHCl2 > EtSiHCl2 >> (EtO)3SiH > Et3SiH.Increase in the electron density on the multiple bond and solvent polarity accelerates the reaction and increases the total yield of the reaction products.Addition of Ph3P and MeCN inhibits hydrosilylation.

HYDROSILYLATION REACTION OF UNSATURATED COMPOUNDS IN THE PRESENCE OF PALLADIUM COMPLEXES

Kopylova, L. I.,Pukhnarevich, V. B.,Tkach, V. S.,Voronkov, M. G.

, p. 904 - 909 (2007/10/02)

The hydrosilylation of 1-hexyne, phenylacetylene, 2-propynyl acetate, 2-propynyl chloride, 1-heptene, and styrene with trichloro-, alkyldichloro-, methyldichloro-, triethyl-, and triethoxysilanes, catalyzed by Pd(0) and Pd(II) complexes, was studied.The hydroxysilylation reaction goes stereospecifically to give two regioisomers, internal (α) and trans-terminal (β), the content of the latter being predominant.The reaction rate grows with increase in the electron-donor power of the ligands on the palladium atom, and with increase in the electronegativity of the substituents on the silicon atom (excluding HSiCl3), in the electron density of the multiple bond, and in the polarity of the solvent.

RUTHENIUM COMPLEXES IN HYDROSILYLATION REACTIONS OF UNSATURATED COMPOUNDS

Kopylova, L. I.,Pukhnarevich, V. B.,Khan, M. M. Tagi,Voronkov, M. G.

, p. 605 - 608 (2007/10/02)

The reactions of trichloro-, alkyldichloro-, triethyl-, and triethoxy-silanes with phenylacetylene catalyzed by Ru(CO)3(PPh3)3, RuH2(CO)(PPh3)3, RuHCl(CO)(PPh3)3, and CpRuCl(PPh3)2, lead mainly to the formation of the terminal adducts PhCH=CHSiRnX3-n (mixtures of the cis and trans isomers).In the case of triethyl- and triethoxy-silanes products of dehydrocondensation PhCCSiR and hydrogenation PhCH2CH2SiR3 (R = Et, OEt) are formed.

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