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Silane, [2-[(4-ethynylphenyl)thio]ethyl]trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

221292-45-1

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221292-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221292-45-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,2,9 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 221292-45:
(8*2)+(7*2)+(6*1)+(5*2)+(4*9)+(3*2)+(2*4)+(1*5)=101
101 % 10 = 1
So 221292-45-1 is a valid CAS Registry Number.

221292-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-ethynylphenyl)sulfanylethyl-trimethylsilane

1.2 Other means of identification

Product number -
Other names HCC-C6H4-S-trimethylsilylethylene

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:221292-45-1 SDS

221292-45-1Relevant academic research and scientific papers

Enhanced Separation Concept (ESC): Removing the Functional Subunit from the Electrode by Molecular Design

Brandl, Thomas,El Abbassi, Maria,Stefani, Davide,Frisenda, Riccardo,Harzmann, Gero D.,van der Zant, Herre S. J.,Mayor, Marcel

, p. 5334 - 5343 (2019/06/21)

A new concept to improve the reliability of functional single molecule junctions is presented using the E-field triggered switching of FeIIbis-terpyridine complexes in a mechanically controlled break junction experiment as model system. The complexes comprise a push-pull ligand sensing the applied E-field and the resulting distortion of the FeII ligand field is expected to trigger a spin-crossover event reflected in a sudden jump of the transport current. By molecular engineering, the active centre of the complex is separated from the gold electrodes in order to eliminate undesired side-effects. Two aspects are considered to isolate the central metal ion, namely the spacing by introducing additional alkynes, and the steric shielding achieved by bulky isopropyl groups. With this small series of model complexes, a pronounced correlation is observed between the occurrence of bistable junctions and the extent of separation of the central metal ion, affirming the hypothesized Enhanced Separation Concept (ESC).

Soluble ferrocene conjugates for incorporation into self-assembled monolayers

Yu,Chong, Yoochul,Kayyem, Jon Faiz,Gozin, Michael

, p. 2070 - 2079 (2007/10/03)

A series of phenylethynyl oligomers (I-V) possessing a ferrocene and thiol at each termini have been synthesized. These oligomers have been designed to overcome the inherent insolubility of this class of complexes by substitution at the phenyl groups with methyl and propoxy substituents. Several new reactions for preparing arenethiol-protected compounds are described. Interestingly, the generation of an arenethiol anion during base- or fluoride-catalyzed deprotection has been characterized.

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