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Tri-n-butylstannyl dichloroacetate is an organotin compound with the chemical formula C12H25Cl2Sn. It is a colorless liquid that is soluble in organic solvents. tri-n-butylstannyl dichloroacetate is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the Stille coupling reaction, a type of cross-coupling reaction. It is also employed as a reducing agent in various chemical processes. Due to its reactivity and potential health and environmental risks, it is important to handle tri-n-butylstannyl dichloroacetate with care, following proper safety protocols.

7299-25-4

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7299-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7299-25-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7299-25:
(6*7)+(5*2)+(4*9)+(3*9)+(2*2)+(1*5)=124
124 % 10 = 4
So 7299-25-4 is a valid CAS Registry Number.

7299-25-4Downstream Products

7299-25-4Relevant academic research and scientific papers

The β-effect with vinyl cations: Kinetic study of the protiodemetalation of silyl-, germyl-, and stannylalkynes

Dallaire, Carol,Brook, Michael A.

, p. 2332 - 2338 (2008/10/08)

The relative magnitude of the hyperconjugative stabilization of vinyl cations by adjacent C-M bonds (M = Si, Ge, Sn; the β-effect) has been examined by measuring the rate constants for the protonation and subsequent protiodemetalation of group 14 metalated (trimethylsilyl)-acetylenes (R3MC≡CSiMe3). The relative β-effect arising from the second-order rate constants Sn ? Ge > Si (maximum kM/kSi = 108, 5 × 102, 1, respectively) follows the same order as that reported for simple carbenium ions. The product ratio from the protonation of Ph3GeC≡CSiMe3 was found to be particularly sensitive to acid concentration and strength, leading to loss of Ph3Ge preferentially with weaker acids. With tin groups, the rate of destannylation decreased with increasing steric bulk, unlike the corresponding situation with silyl groups. The origins of both these observations may be attributed to nucleophilic interaction at the metal center during protonation.

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