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(E)-1-(Chlorodimethylsilyl)-2-(trimethylsilyl)ethene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28714-29-6

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28714-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28714-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,7,1 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28714-29:
(7*2)+(6*8)+(5*7)+(4*1)+(3*4)+(2*2)+(1*9)=126
126 % 10 = 6
So 28714-29-6 is a valid CAS Registry Number.

28714-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-1-(Chlordimethylsilyl)-2-(trimethylsilyl)ethen

1.2 Other means of identification

Product number -
Other names (E)-1-(Chloro-dimethyl-silanyl)-2-trimethylsilanyl-ethene

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:28714-29-6 SDS

28714-29-6Downstream Products

28714-29-6Relevant academic research and scientific papers

Sila-pheromones: Silicon analogues of the female sex pheromone of the processionary moth Thaumetopoea pityocampa

Arsequell, Gemma,Camps, Francisco,Fabrias, Gemma,Guerrero, Angel

, p. 2739 - 2742 (1990)

The 15- and 10-dimethylsila-analogues of (Z)-13-hexadecen-11-ynyl acetate, the main component of the female sex pheromone of the processionary moth Thaumetopoea pityocampa, were synthesized to evaluate the influence of the silicon atom on the biological activity.

Synthesis and Spectroscopic Characterization of Di- and Trisilylethenes

Schmidbaur, H.,Ebenhoech, J.

, p. 1543 - 1548 (2007/10/02)

Di- and trisilylethenes have been prepared by catalytic hydrosilylation of trimethylsilyl-, bis(trimethylsilyl)- and bis(trichlorosilyl)ethyne and converted into the hydrogenated derivatives by LiAlH4-reduction.The stereochemistry of the products and the effects of substitution of methyl vs. chlorine ligands on the NMR coupling constants J(29Si/1H) have been investigated by analysis of selectively (Me)-decoupled 29Si NMR spectra.From the results it has been concluded, that the catalytic hydrosilylation of silylated ethynes proceeds in a stereospecific syn fashion yield ing trans adducts.Substitution of methyl by chlorine at one or two Si-atoms in tris(trimethylsilyl)ethene leads to an increase of the coupling constant J(29Si/1H vinyl) with the chlorinated Si-atoms and reduces the values for those Si-atoms, where the methyl groups are retained. - Keywords: Di- and Trisilylethenes, Catalytic Hydrosilylation

UNUSUAL REGIOSELECTIVE HYDROSILYLATION OF ETHYNYLMETHYLDICHLOROSILANE WITH DIMETHYILCHLOROSILANE CATALYZED BY TETRAKIS(TRIPHENYLPHOSPHINE)PLATINUM(O)

Matsumoto, Hideyuki,Hoshino, Yoshikazu,Nagai, Yoichiro

, p. 1663 - 1666 (2007/10/02)

The hydrosilylation of ethynylmethyldichlorosilane with dimethylchlorosilane catalyzed by tetrakis(triphenylphosphine)platinum(O) was found to show quite an unusual regioselectivity to afford the geminal product, 1-(methyldichlorosilyl)-1-(dimethylchlorosilyl)ethene, almost exclusively.

ADDITION OF CHLORODISILANES TO ACETYLENE CATALYZED BY TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM(0). A FACILE ROUTE TO (Z)-1,2-BIS(CHLOROSILYL)ETHENES

Matsumoto, Hideyuki,Matsubara, Ikuya,Kato, Takayuki,Shono, Koichi,Watanabe, Hamao,Nagai, Yoichiro

, p. 43 - 48 (2007/10/02)

In the presence of a catalytic amount of tetrakis(triphenylphosphine)palladium(0), chlorodisilanes of type MenSi2Cl6-n (n=2-5) add to acetylene to afford 1,2-bis(chlorosilyl)ethenes in reasonable yields.

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