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N,N-dimethyl-N′-tosylbenzimidamide, also known as TosMIC, is an organic compound with the chemical formula C15H18N2O2S. It is a valuable reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the Michael addition reaction. TosMIC is a masked form of the imidate ion, which is generated in situ by the deprotonation of TosMIC with a strong base. This intermediate is highly reactive and can readily react with various Michael acceptors, such as α,β-unsaturated carbonyl compounds, to form new carbon-carbon bonds. The tosyl group (Ts) serves as a protecting group for the nitrogen atom, enhancing the reactivity of the imidate ion and facilitating the reaction. TosMIC is widely used in the synthesis of various natural products, pharmaceuticals, and other complex organic molecules due to its high reactivity and selectivity.

4115-23-5

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4115-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4115-23-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,1 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4115-23:
(6*4)+(5*1)+(4*1)+(3*5)+(2*2)+(1*3)=55
55 % 10 = 5
So 4115-23-5 is a valid CAS Registry Number.

4115-23-5Downstream Products

4115-23-5Relevant academic research and scientific papers

Synthesis of N-Sulfonyl Amidines and Acyl Sulfonyl Ureas from Sulfonyl Azides, Carbon Monoxide, and Amides

Chow, Shiao Y.,Odell, Luke R.

, p. 2515 - 2522 (2017)

A Pd-catalyzed and ligand-free carbonylation/cycloaddition/decarboxylation cascade synthesis of sulfonyl amidines from sulfonyl azides and substituted amides at low CO pressure is reported. The reaction proceeds via an initial Pd-catalyzed carbonylative generation of sulfonyl isocyanates from sulfonyl azides, followed by a [2 + 2] cycloaddition with amides and subsequent decarboxylation, which liberates the desired sulfonyl amidines, generating N2 and CO2 as the only reaction byproducts. Using this simple protocol, a diverse range of sulfonyl amidines was obtained in moderate to excellent yields. In addition, the reaction can also be directed through a more conventional amidocarbonylation pathway by employing N-monosubstituted amide nucleophiles to afford acyl sulfonyl ureas in good yields.

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