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N-(3-methoxypropyl)-4-methylbenzenesulfonamide is a chemical compound with the molecular formula C11H17NO3S. It is an organic molecule that belongs to the class of sulfonamides, which are known for their diverse applications in various fields, including pharmaceuticals and dyes. This specific compound features a benzene ring with a methyl group at the 4-position and a sulfonamide group attached to a 3-methoxypropyl chain. The presence of the methoxy group provides a hydroxyl group with an ether linkage, which can influence the compound's solubility and reactivity. The compound's structure and properties make it a potential candidate for further study in chemical research and development, particularly in the context of its potential applications and interactions within complex chemical systems.

885-02-9

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885-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 885-02-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 885-02:
(5*8)+(4*8)+(3*5)+(2*0)+(1*2)=89
89 % 10 = 9
So 885-02-9 is a valid CAS Registry Number.

885-02-9Relevant academic research and scientific papers

Catalyst-Free Visible-Light-Mediated Iodoamination of Olefins and Synthetic Applications

Engl, Sebastian,Reiser, Oliver

supporting information, p. 5581 - 5586 (2021/07/26)

Herein we report a catalyst- and metal-free visible-light-mediated protocol enabling the iodoamination of miscellaneous olefins. This protocol is characterized by high yields under environmentally benign reaction conditions utilizing commercially available substrates and a green and biodegradable solvent. Furthermore, the protocol allows for late-stage functionalization of bioactive molecules and can be scaled to gram quantities of product, which offers manifold possibilities for further transformations, including morpholine, piperidine, pyrrolidine, and aziridine synthesis.

Transition-Metal-Free One-Step Synthesis of Ynamides

Zeng, Xianzhu,Tu, Yongliang,Zhang, Zhenming,You, Changming,Wu, Jiao,Ye, Zhiying,Zhao, Junfeng

, p. 4458 - 4466 (2019/03/26)

A robust transition-metal-free one-step strategy for the synthesis of ynamides from sulfonamides and (Z)-1,2-dichloroalkenes or alkynyl chlorides is presented. This method is not only effective for internal ynamides but also amenable for terminal ynamides. Various functional groups, even the vinyl moiety, are compatible, and thus, this strategy offers the opportunity for further functionalization.

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