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(Z)-t-butyl 3-phenyl-2-(tri-n-butylstannyl)propenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98830-92-3

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98830-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98830-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,8,3 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98830-92:
(7*9)+(6*8)+(5*8)+(4*3)+(3*0)+(2*9)+(1*2)=183
183 % 10 = 3
So 98830-92-3 is a valid CAS Registry Number.

98830-92-3Relevant academic research and scientific papers

Synthesis of α-stannyl α,β-unsaturated carboxylic esters

Zapata, Antonio J.,Fortoul R., Corina,Acuna A., Carola

, p. 69 - 74 (2007/10/02)

A synthetic method for the preparation of α-stannyl α,β-unsaturated esters is described.The lithium enolate derived from tert-butyl α-(tri-n-butylstannyl)-α-(trimethylsilyl)acetate reacts with aldehydes to give moderate to good yields of α-stannylated products.The method is not applicable to enolizable ketones.

Reactions of t-butyl (trialkylstannyl)(trimethylgermyl)acetates and application of their anions to the Peterson-type reaction

Kanemoto, Naohide,Sato, Yoshiro,Inoue, Sumie

, p. 25 - 32 (2007/10/02)

Three t-butyl (trialkylstannyl)(trimethylgermyl)acetates were synthesized and subjected to the Peterson-type reaction with carbonyl compounds. t-Butyl 2-(trimethylgermyl)-2-alkenoates were obtained as the main products from (tri-n-butyl-stannyl)-2-alkenoates and 2-alkenoates as minor products.

Preparation of vinylstannanes via the Peterson reaction

Ager, David J.,Cooke, Glen E.,East, Michael B.,Mole, Susan J.,Rampersaud, Ashraff,Webb, Victoria J.

, p. 1906 - 1908 (2008/10/08)

The condensation of anions derived from (phenylthio)(tri-n-butylstannyl)(trimethylsilyl)methane (2a), tert-butyl (tri-n-butylstannyl)(trimethylsilyl)acetate (2b), and (tri-n-butylstannyl)(trimethylsilyl)methane (2c) with carbonyl compounds was used to com

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