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(3,5-dimethylphenyl)trimethylstannane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

260269-19-0

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260269-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 260269-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,2,6 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 260269-19:
(8*2)+(7*6)+(6*0)+(5*2)+(4*6)+(3*9)+(2*1)+(1*9)=130
130 % 10 = 0
So 260269-19-0 is a valid CAS Registry Number.

260269-19-0Downstream Products

260269-19-0Relevant academic research and scientific papers

Visible-Light-Driven Synthesis of Arylstannanes from Arylazo Sulfones

Lian, Chang,Yue, Guanglu,Mao, Jinshan,Liu, Danyang,Ding, Yi,Liu, Zerong,Qiu, Di,Zhao, Xia,Lu, Kui,Fagnoni, Maurizio,Protti, Stefano

supporting information, p. 5187 - 5191 (2019/07/03)

The visible-light-driven preparation of (hetero)aryl stannanes was carried out under both photocatalyst- and metal-free conditions via irradiation of arylazo sulfones in the presence of hexaalkyldistannanes. The reaction shows a high efficiency and a wide substrates scope. The resulting crude organotin derivatives can be directly employed in a Stille protocol.

Synthesis of 1,3,5-tri- and 1,2,4,5-tetrasubstituted tin and mercury derivatives of benzene. Crystal structure of 1,3,5-tris(chloromercurio)benzene

Rot, Nicolette,De Kanter, Frans J.J.,Bickelhaupt, Friedrich,Smeets, Wilberth J.J.,Spek, Anthony L.

, p. 369 - 379 (2007/10/03)

The reaction of 1,3,5-tribromo- or 1,2,4,5-tetrabromobenzene with trimethylstannyl sodium in tetraglyme gave the corresponding polystannylated benzene derivatives 2 and 4, respectively, in high yield. They were converted with mercuric chloride to the corresponding tris- and tetrakis(chloromercurio)benzenes 5 and 6, respectively. The structure of 5 was confirmed by X-ray crystallography. Some spectral properties of the new compounds are discussed. The (partial) conversion of 2 to 1,3,5-trilithiobenzene (8) was also investigated.

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