26103-48-0 Usage
Uses
Used in Pharmaceutical Research:
4-(Pyridin-3-ylsulphonyl)morpholine is used as a reagent in pharmaceutical research for its potential medicinal properties. It is being explored as an enzyme inhibitor, which could have implications for the development of treatments targeting specific diseases.
Used in Organic Synthesis:
In the field of organic synthesis, 4-(Pyridin-3-ylsulphonyl)morpholine is utilized as a building block for the synthesis of other complex molecules. Its unique structure allows it to be a key component in creating new compounds with various applications.
Used in Disease Treatment:
4-(Pyridin-3-ylsulphonyl)morpholine is being investigated for its potential use in the treatment of various diseases. Its enzyme inhibitory activity suggests that it could play a role in managing or treating conditions related to enzyme dysregulation.
Used in Chemical Research:
Due to its unique structure and potential for versatile applications, 4-(Pyridin-3-ylsulphonyl)morpholine is of interest to researchers in the field of chemistry. It provides opportunities for studying new reactions and exploring its behavior in different chemical environments.
Check Digit Verification of cas no
The CAS Registry Mumber 26103-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,0 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 26103-48:
(7*2)+(6*6)+(5*1)+(4*0)+(3*3)+(2*4)+(1*8)=80
80 % 10 = 0
So 26103-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O3S/c12-15(13,9-2-1-3-10-8-9)11-4-6-14-7-5-11/h1-3,8H,4-7H2
26103-48-0Relevant academic research and scientific papers
Copper-catalyzed electrophilic amination of sodium sulfinates at room temperature
Zhu, Haibo,Shen, Yajing,Deng, Qinyue,Tu, Tao
supporting information, p. 16573 - 16576 (2015/11/18)
By using O-benzoyl hydroxylamines as amine sources, the first convenient copper-catalyzed electrophilic amination of sodium sulfinates has been realized. Even with 2 mol% catalyst loading, the protocol provided an efficient and straightforward synthesis of a broad range of functional sulfonamides under ambient reaction conditions without an additional base and ligand. Based on the control experiments, a plausible mechanism was proposed.
A general and mild two-step procedure for the synthesis of aryl and heteroaryl sulfonamides from the corresponding iodides
Ho, Danny K.H.,Chan, Lily,Hooper, Alice,Brennan, Paul E.
, p. 820 - 823 (2011/03/18)
A mild two-step preparation of aryl and heteroaryl sulfonyl chlorides and sulfonamides from their corresponding iodides is developed. Acid labile functionalities are shown to be stable under both the copper-catalysed coupling and the subsequent oxidative chlorination.
Acetyl-CoA carboxylase inhibitors
-
, (2008/06/13)
Acetyl Coenzyme A Carboxylase inhibitors, pharmaceutical compositions containing such compounds and the use of such compounds to treat for example, Metabolic Syndrome including atherosclerosis, diabetes and obesity.
