2374225-98-4 Usage
Uses
Used in Medicinal Chemistry:
(Rs)-N-((Sc)-(5-(diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(o-tolyl)methyl)-2-methylpropane-2-sulfinamide is used as a potential candidate in medicinal chemistry for its unique structural features and the possibility of interacting with biological targets due to its complex functional groups.
Used in Organic Synthesis:
In the field of organic synthesis, (Rs)-N-((Sc)-(5-(diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(o-tolyl)methyl)-2-methylpropane-2-sulfinamide may serve as a key intermediate or a building block for the synthesis of other complex organic molecules, taking advantage of its reactive functional groups and structural diversity.
Used in Pharmaceutical Research:
Within the pharmaceutical industry, (Rs)-N-((Sc)-(5-(diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(o-tolyl)methyl)-2-methylpropane-2-sulfinamide could be utilized in the development of new drugs, potentially targeting various diseases by leveraging its unique chemical properties and interactions with biological systems.
Used in Chemical Research:
(Rs)-N-((Sc)-(5-(diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(o-tolyl)methyl)-2-methylpropane-2-sulfinamide may also be employed in chemical research to study the effects of its structural components on reactivity, stability, and other chemical behaviors, contributing to the broader understanding of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 2374225-98-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,3,7,4,2,2 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2374225-98:
(9*2)+(8*3)+(7*7)+(6*4)+(5*2)+(4*2)+(3*5)+(2*9)+(1*8)=174
174 % 10 = 4
So 2374225-98-4 is a valid CAS Registry Number.
2374225-98-4Relevant academic research and scientific papers
Pd/PC-Phos-Catalyzed Enantioselective Intermolecular Denitrogenative Cyclization of Benzotriazoles with Allenes and N-Allenamides
Zhang, Pei-Chao,Han, Jie,Zhang, Junliang
, p. 11444 - 11448 (2019/07/17)
Reported herein is an asymmetric Pd/PC-Phos-catalyzed denitrogenative cyclization of benzotriazoles with allenes and N-allenamides, representing the first example of enantioselective denitrogenative cyclizations of benzotriazoles. A series of optically active 3-methyleneindolines were obtained in good yields with high ee values. The use of inexpensive and readily available starting materials, high regio- and enantioselectivity, a broad substrate scope, mild reaction conditions, no need for base, as well as versatile functionalization of the 3-methyleneindolines make this approach attractive.
