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Silane, [(5-ethyl-3-thienyl)ethynyl]trimethyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

467251-52-1

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467251-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 467251-52-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,7,2,5 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 467251-52:
(8*4)+(7*6)+(6*7)+(5*2)+(4*5)+(3*1)+(2*5)+(1*2)=161
161 % 10 = 1
So 467251-52-1 is a valid CAS Registry Number.

467251-52-1Downstream Products

467251-52-1Relevant academic research and scientific papers

Tandem catalytic C(sp3)-H amination/sila-sonogashira-hagihara coupling reactions with iodine reagents

Buendia, Julien,Darses, Benjamin,Dauban, Philippe

supporting information, p. 5697 - 5701 (2015/06/16)

A new tandem C-N and C-C bond-forming reaction has been achieved through RhII/Pd0 catalysis. The sequence first involves an iodine(III) oxidant, then the in situ generated iodine(I) by-product is used as a coupling partner. The overall process demonstrates the synthetic value of iodoarenes produced in trivalent iodine reagent mediated oxidations. I(003) is a double agent: A tandem C-N and C-C bond-forming reaction has been achieved through RhII/Pd0 catalysis. The sequence first involves an iodine(III) oxidant, then the in situ generated iodine(I) by-product is used as a coupling partner. The overall process affords complex building blocks with high yields, and demonstrates the synthetic value of iodoarenes produced in trivalent iodine reagent mediated oxidations.

Synthesis and properties of coil-shaped 2,3-thienylene-ethynylene oligomers

Aso, Yoshio,Obara, Yuko,Okai, Takashi,Nishiguchi, Shoji,Otsubo, Tetsuo

, p. 153 - 158 (2007/10/03)

A series of 2,3-thienylene-ethynylene oligomers have been synthesized by repeated application of the Pd-catalyzed coupling reaction of terminal alkynes and thienyl iodides as the key building steps. The analytical GPC molecular weights, much deflated relative to the actual molecular weights, strongly suggest a coil shape for the conformation of the oligomers in solution. Their electronic absorption and emission spectral features are discussed.

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