13904-95-5 Usage
Description
(methylsulfonodiimidoyl)methane, also known as Methylsulfonylmethanimidamide, is a chemical compound characterized by its molecular formula C3H9N3O2S. This colorless liquid at room temperature is recognized for its utility as a reagent in the realms of organic synthesis and pharmaceutical research. Beyond its synthetic applications, (methylsulfonodiimidoyl)methane has garnered attention for its potential therapeutic and pharmacological properties, with research indicating possible anti-inflammatory, analgesic, and antioxidant effects. Studies are also exploring its efficacy in addressing various conditions, including arthritis, tendon disorders, and other inflammatory diseases.
Uses
Used in Pharmaceutical Research:
(methylsulfonodiimidoyl)methane serves as a crucial reagent in the field of pharmaceutical research, facilitating the development of novel drugs and therapies. Its unique chemical structure allows for its use in the synthesis of complex molecules, contributing to the advancement of medicinal chemistry.
Used in Organic Synthesis:
As a versatile reagent in organic synthesis, (methylsulfonodiimidoyl)methane aids in the creation of a wide array of organic compounds. Its ability to participate in various chemical reactions makes it an invaluable tool for chemists working on the development of new materials and substances.
Used in Anti-inflammatory Applications:
Given its potential anti-inflammatory properties, (methylsulfonodiimidoyl)methane is being investigated for use in the treatment of conditions characterized by inflammation, such as arthritis and tendon disorders. Its ability to potentially alleviate inflammation could make it a valuable asset in the management of these conditions.
Used in Analgesic Applications:
The analgesic potential of (methylsulfonodiimidoyl)methane is another area of interest, as it may provide relief from pain associated with various conditions. Further research is necessary to fully understand its efficacy and safety in this application.
Used in Antioxidant Applications:
The antioxidant properties of (methylsulfonodiimidoyl)methane suggest that it may play a role in protecting cells from damage caused by reactive oxygen species. This could have implications for the treatment and prevention of a range of diseases and conditions associated with oxidative stress.
Used in the Treatment of Inflammatory Conditions:
Ongoing research is exploring the use of (methylsulfonodiimidoyl)methane in the treatment of various inflammatory conditions. Its potential to reduce inflammation and alleviate associated symptoms positions it as a promising candidate for further study and potential therapeutic application.
Check Digit Verification of cas no
The CAS Registry Mumber 13904-95-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,0 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13904-95:
(7*1)+(6*3)+(5*9)+(4*0)+(3*4)+(2*9)+(1*5)=105
105 % 10 = 5
So 13904-95-5 is a valid CAS Registry Number.
InChI:InChI=1/C2H8N2S/c1-5(2,3)4/h3-4H,1-2H3
13904-95-5Relevant articles and documents
Sulfoximines from a Medicinal Chemist's Perspective: Physicochemical and in vitro Parameters Relevant for Drug Discovery
Frings, Marcus,Bolm, Carsten,Blum, Andreas,Gnamm, Christian
supporting information, p. 225 - 245 (2016/11/19)
Sulfoximines, sulfondiimides and sulfonimidamides are fascinating but not yet fully explored variants of the common sulfone or sulfonamide motif. In this study, we report the physicochemical and in vitro properties of sulfoximines and compare them with related analogs and isosteres. Furthermore, we present a matched molecular pair analysis of compounds from drug discovery projects within Boehringer Ingelheim. We demonstrate that the sulfoximine moiety is a chemically stable, comparatively polar and weakly basic functional group, often leading to favorable aqueous solubility, permeability and metabolic stability. Moreover, their additional vectors at nitrogen enable simple chemical modifications and thus facilitate exploration and fine-tuning of the molecular properties. We conclude that sulfoximines and their congeners do not exhibit any intrinsic flaw but significantly enrich the toolbox of medicinal chemists.
