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

123382-30-9

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123382-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123382-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,3,8 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 123382-30:
(8*1)+(7*2)+(6*3)+(5*3)+(4*8)+(3*2)+(2*3)+(1*0)=99
99 % 10 = 9
So 123382-30-9 is a valid CAS Registry Number.

123382-30-9SDS

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 (Z)-2-(4-methylphenylethenyl)trimethylsilane

1.2 Other means of identification

Product number -
Other names Trimethyl-((Z)-2-p-tolyl-vinyl)-silane

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:123382-30-9 SDS

123382-30-9Downstream Products

123382-30-9Relevant academic research and scientific papers

Synthesis of multinuclear Rh(I) complexes bearing triazolylidenes and their application in C-C and c-Si bond forming reactions

Mendoza-Espinosa, Daniel,Rendón-Nava, David,Vásquez-Pérez, Jose M.,Sandoval-Chávez, Cesar I.,Alvarez-Hernández, Alejandro

, p. 3961 - 3971 (2020/12/01)

Multidentate carbene ligands are valuable frameworks for the preparation of carbene complexes displaying higher nuclearity. In the present work, we report the synthesis of a series of mono- to tetra-[Rh(COD)I] complexes (3a- d) supported by mesoionic triazol-5-ylidenes. The general synthetic procedure involves the one step reaction of the appropriate triazolium (2a-d) salt in the presence of KHMDS and stoiquiometric amounts of the rhodium(I) precursor. Treatment of complexes 3a-d with an excess of carbon monoxide allows for the quantitative preparation of complexes 4a-d featuring a [Rh(CO)2I] fragment used for the detemination of the donor properties of the new triazolylidene ligands. All complexes have been fully characterized by means of 1H and 13C NMR spectroscopy, melting point, elemental analysis, and in the case of complex 3a, by X-ray crystallography. Comparison of the catalytic activity of the new rhodium complexes in C-C and C-Si bond forming processes demonstrate the enhanced performance of the tetranuclear species suggesting the possibility of strong cooperative effects in these multinuclear complexes.

Synthesis of (E)-alkenes via hydroindation of C{triple bond, long}C in InCl3-NaBH4 system

Wang, Chunyan,Yan, Lei,Zheng, Zhiguo,Yang, Deyu,Pan, Yuanjiang

, p. 7712 - 7717 (2007/10/03)

In InCl3-NaBH4-MeCN system, terminal aryl alkynes could couple with aryl iodides and bromides to give disubstituted alkenes via hydroindation of C{triple bond, long}C. In the similar way, (E)-alkenylsilanes were synthesized via reduction of alkynylsilanes in tetrahydrofuran (THF) in high yields. The processes showed high regio- and stereoselectivity.

TRIMETHYLSILYLDIAZOMETHANE: A USEFUL REAGENT FOR THE PREPARATION OF (Z)-1-TRIMETHYLSILYL-1-ALKENES

Aoyama, Toyohiko,Shioiri, Takayuki

, p. 2261 - 2262 (2007/10/02)

The rhodium(II) pivalate-catalysed decomposition of α-trimethylsilyldiazoalkenes stereoselectivity affords (Z)-1-trimethylsilyl-1-alkenes in good yields.Keywords trimethylsilyldiazomethane; α-trimethylsilyldiazoalkane; (Z)-1-trimethylsilyl-1-alkene; rhodium(II) pivalate; catalytic decomposition

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