86864-35-9 Usage
Description
1-(4-methoxyphenyl)-N-(tritylsulfanyl)methanimine is a chemical compound characterized by its molecular formula C22H21NOS and a molar mass of 351.47 g/mol. It is a methoxyphenyl-substituted imine derivative featuring a trityl-protected thiol group. 1-(4-methoxyphenyl)-N-(tritylsulfanyl)methanimine holds potential in the realms of organic synthesis and medicinal chemistry due to its reactivity and functional groups, which can be harnessed for the creation of diverse organic molecules and pharmaceuticals. Additionally, its structural features suggest possible biological activities, making it a promising candidate for further research and development within the chemical and pharmaceutical sciences.
Uses
Used in Organic Synthesis:
1-(4-methoxyphenyl)-N-(tritylsulfanyl)methanimine is used as a synthetic intermediate for the creation of various organic molecules. Its unique functional groups and reactivity allow for the development of a wide range of compounds with potential applications in different industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(4-methoxyphenyl)-N-(tritylsulfanyl)methanimine is used as a key building block for the synthesis of pharmaceuticals. Its structural features and potential biological activities make it a valuable compound for the development of new drugs and therapeutic agents.
Used in Chemical Research:
1-(4-methoxyphenyl)-N-(tritylsulfanyl)methanimine is also utilized as a research compound in the field of chemical sciences. Its unique properties and potential applications make it an interesting subject for further study, with the aim of uncovering new insights and advancements in chemical synthesis and understanding of its biological activities.
Used in Pharmaceutical Sciences:
Within the pharmaceutical sciences, 1-(4-methoxyphenyl)-N-(tritylsulfanyl)methanimine is used as a compound with potential therapeutic applications. Its structural features and reactivity may contribute to the development of novel drugs and therapeutic agents, particularly in the areas of organic synthesis and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 86864-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,6 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86864-35:
(7*8)+(6*6)+(5*8)+(4*6)+(3*4)+(2*3)+(1*5)=179
179 % 10 = 9
So 86864-35-9 is a valid CAS Registry Number.
86864-35-9Relevant articles and documents
Studies on the Preparation and Reactions of Tritylsulfenimines
Branchaud, Bruce P.
, p. 3531 - 3538 (2007/10/02)
Carbonyl compounds react with stable, crystalline triphenylmethanesulfenamide (TrSNH2, 4) under mild conditions to form tritylsulfenimines 5 and 6.Lithiation of acetone tritylsulfenimine (5c) at O deg C led to a novel rearrangement-decomposition producing
