13904-95-5 Usage
General Description
(methylsulfonodiimidoyl)methane, also known as Methylsulfonylmethanimidamide, is a chemical compound with the molecular formula C3H9N3O2S. It is a colorless liquid at room temperature, and it is commonly used as a reagent in organic synthesis and pharmaceutical research. (methylsulfonodiimidoyl)methane is also known for its potential therapeutic and pharmacological properties, with studies suggesting that it may have anti-inflammatory, analgesic, and antioxidant effects. Additionally, (methylsulfonodiimidoyl)methane has been investigated for its potential use in the treatment of conditions such as arthritis, tendon disorders, and other inflammatory conditions. Further research and clinical trials are ongoing to explore the full range of its medical and industrial applications.
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.
