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4-amino-N-(2-o-tolyl-2H-pyrazol-3-yl)-benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13117-40-3

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13117-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13117-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,1 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13117-40:
(7*1)+(6*3)+(5*1)+(4*1)+(3*7)+(2*4)+(1*0)=63
63 % 10 = 3
So 13117-40-3 is a valid CAS Registry Number.

13117-40-3Downstream Products

13117-40-3Relevant academic research and scientific papers

Aromatic C-H Methylation and Other Functionalizations via the Rh(III)-Catalyzed Migratory Insertion of Bis(phenylsulfonyl)carbene and Subsequent Transformations

Chen, Lei,Peng, Rui-Jun,Zhang, Xue-Jing,Yan, Ming,Chan, Albert S. C.

, p. 10177 - 10189 (2021/07/28)

The Rh(III)-catalyzed migratory insertion of bis(phenylsulfonyl)carbene into aromatic C-H bonds has been developed. A variety of bis(phenylsulfonyl)methyl derivatives were prepared with good yields under mild conditions. The methylated products were readily obtained after reductive desulfonylation. Furthermore, the diverse transformations of bis(phenylsulfonyl)methyl to trideuteriomethyl, aldehyde, and other functional groups were demonstrated.

Cobalt-catalysed C–H methylation for late-stage drug diversification

Ackermann, Lutz,Friis, Stig D.,Johansson, Magnus J.

, p. 511 - 519 (2020/06/05)

The magic methyl effect is well acknowledged in medicinal chemistry, but despite its significance, accessing such analogues via derivatization at a late stage remains a pivotal challenge. In an effort to mitigate this major limitation, we here present a strategy for the cobalt-catalysed late-stage C–H methylation of structurally complex drug molecules. Enabling broad applicability, the transformation relies on a boron-based methyl source and takes advantage of inherently present functional groups to guide the C–H activation. The relative reactivity observed for distinct classes of functionalities were determined and the sensitivity of the transformation towards a panel of common functional motifs was tested under various reaction conditions. Without the need for prefunctionalization or postdeprotection, a diverse array of marketed drug molecules and natural products could be methylated in a predictable manner. Subsequent physicochemical and biological testing confirmed the magnitude with which this seemingly minor structural change can affect important drug properties. [Figure not available: see fulltext.]

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