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((4-chlorophenyl)ethynyl)triethylsilane is an organosilicon compound characterized by a unique structure that combines a 4-chlorophenyl group with an ethynyl (acetylene) moiety, which is further attached to a triethylsilyl group. ((4-chlorophenyl)ethynyl)triethylsilane is of interest in organic synthesis and materials science due to its potential applications in the formation of various organic molecules and its ability to influence the properties of materials through its incorporation. The presence of the chlorine atom on the phenyl ring allows for further functionalization, while the ethynyl group can participate in cross-coupling reactions, making ((4-chlorophenyl)ethynyl)triethylsilane a versatile building block in synthetic chemistry.

4131-56-0

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4131-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4131-56-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,3 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4131-56:
(6*4)+(5*1)+(4*3)+(3*1)+(2*5)+(1*6)=60
60 % 10 = 0
So 4131-56-0 is a valid CAS Registry Number.

4131-56-0Relevant academic research and scientific papers

Cationic dirhodium carboxylate-catalyzed synthesis of dihydropyrimidones from propargyl ureas

Yang, Miao,Odelberg, Shannon J.,Tong, Zongzhong,Li, Dean Y.,Looper, Ryan E.

supporting information, p. 5744 - 5750 (2013/06/27)

Cationic Rh(II) complexes are able to catalyze the regioselective hydroamination of propargyl ureas in a 6-endo fashion. This transformation permits access to interesting substitution patterns of dihydropyrimidines, which have found use as nucleotide exch

Pd-EnCat TPP30 as a catalyst for the generation of highly functionalized aryl- and alkenyl-substituted acetylenes via microwave-assisted sonogashira type reactions

Sedelmeier, Joerg,Ley, Steven V.,Lange, Heiko,Baxendale, Ian R.

supporting information; experimental part, p. 4412 - 4420 (2010/01/07)

We report a rapid microwave-assisted Sonogashira crosscoupling of aryl iodides and bromides with terminal alkynes using Pd-EnCat TPP30. Both electron-rich and electrondeficient aryl halides reacted smoothly with a broad variety of terminal alkynes in MeCN

Homogeneous catalysts supported on soluble polymers: Biphasic Sonogashira coupling of aryl halides and acetylenes using MeOPEG-bound phosphine - Palladium catalysts for efficient catalyst recycling

Koellhofer, Axel,Plenio, Herbert

, p. 1416 - 1425 (2007/10/03)

The Sonogashira coupling of various aryl bromides and iodides with different acetylenes was studied under biphasic conditions with soluble, polymer-modified catalysts to allow the efficient recycling of the homogeneous catalyst. For this purpose, several

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