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5033-21-6

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5033-21-6 Usage

General Description

4-(Phenylsulfonyl)Morpholine, 97% is a chemical compound that is commonly used in organic synthesis and pharmaceutical research. It is a high purity, 97% grade of the compound, which indicates that it is suitable for use in a variety of applications. 4-(Phenylsulfonyl)Morpholine, 97% is a morpholine derivative with a phenylsulfonyl group attached, and it has potential uses in the development of new pharmaceuticals and agrochemicals. It is also used as a building block in the synthesis of various organic molecules and can be employed in the preparation of diverse types of heterocyclic compounds. With its high purity and versatile chemical properties, 4-(Phenylsulfonyl)Morpholine, 97% is a valuable tool for researchers and chemists working in the field of organic chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 5033-21-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,3 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5033-21:
(6*5)+(5*0)+(4*3)+(3*3)+(2*2)+(1*1)=56
56 % 10 = 6
So 5033-21-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3S/c12-15(13,10-4-2-1-3-5-10)11-6-8-14-9-7-11/h1-5H,6-9H2

5033-21-6Downstream Products

5033-21-6Relevant articles and documents

AEROBIC OXIDATIVE SYNTHESIS OF SULFONAMIDE USING Cu CATALYST

-

, (2021/04/06)

The present invention relates to a method for oxidative synthesis of sulfonamides using copper catalysts. , Oxygen (O) is used. 2 The oxidative synthesis of sulfonamides (1) comprises reacting a 2 th or sulfonyl hydrazide primary amine with a sulfonyl hydrazide (sulfonamide) with a copper catalyst on a solvent under the conditions in which the sulphonamide is fed. The oxidation coupling of the present invention showed extensive substrate ranges in an amine comprising a 2 primary amine, 1 primary amine and amine hydrochloride salt. It is worth notable that non-reactive aliphatic sulfonyl hydrazides in previously reported anaerobic systems can be used for the aerobic oxidation coupling of the present invention. The oxidation coupling of the present invention has been more effective on large scale.

Structure–activity relationships (SARs) of α- ketothioamides as inhibitors of phosphoglycerate dehydrogenase (PHGDH)

Spillier, Quentin,Ravez, Séverine,Unterlass, Judith,Corbet, Cyril,Degavre, Charline,Feron, Olivier,Frédérick, Rapha?l

, (2020/02/11)

For many years now, targeting deregulation within cancer cells’ metabolism has appeared as a promising strategy for the development of more specific and efficient cancer treatments. Recently, numerous reports highlighted the crucial role of the serine synthetic pathway, and particularly of the phosphoglycerate dehydrogenase (PHGDH), the first enzyme of the pathway, to sustain cancer progression. Yet, because of very weak potencies usually in cell-based settings, the inhibitors reported so far failed to lay ground on the potential of this approach. In this paper, we report a structure–activity relationship study of a series of α-ketothioamides that we have recently identified. Interestingly, this study led to a deeper understanding of the structure–activity relationship (SAR) in this series and to the identification of new PHGDH inhibitors. The activity of the more potent compounds was confirmed by cellular thermal shift assays and in cell-based experiments. We hope that this research will eventually provide a new entry point, based on this promising chemical scaffold, for the development of therapeutic agents targeting PHGDH.

Efficient and Practical Synthesis of Sulfonamides Utilizing SO2 Gas Generated on Demand

Chung Leung, Gulice Yiu,Ramalingam, Balamurugan,Loh, Gabriel,Chen, Anqi

, p. 546 - 554 (2020/04/22)

A simple and practical protocol was developed for the synthesis of sulfonamides by reacting organometallic reagents with SO2 gas generated on demand. SO2 was generated from readily available reagents safely in a highly contained and controlled fashion. The protocol allows the synthesis of sulfonamides without using either atom-inefficient SO2 surrogates or a SO2 cylinder that requires stringent storage regulations in the laboratory. The protocol was successfully applied to the synthesis of sildenafil.

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