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1841512-58-0

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1841512-58-0 Usage

Derivative of

1,3-dioxoisoindoline

Attached group

Phenylbutanoate group to the nitrogen atom

Common use

Organic synthesis and medicinal chemistry

Building block for

Preparation of pharmaceuticals (e.g., antipsychotic and anti-inflammatory drugs)

Additional role

Catalyst or reagent in chemical reactions

Potential applications

Drug discovery and development

Relevance

Study of organic and pharmaceutical chemistry

Structural features

Unique, contributing to its potential in various applications

Check Digit Verification of cas no

The CAS Registry Mumber 1841512-58-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,4,1,5,1 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1841512-58:
(9*1)+(8*8)+(7*4)+(6*1)+(5*5)+(4*1)+(3*2)+(2*5)+(1*8)=160
160 % 10 = 0
So 1841512-58-0 is a valid CAS Registry Number.

1841512-58-0Relevant articles and documents

Expanding Reactivity in DNA-Encoded Library Synthesis via Reversible Binding of DNA to an Inert Quaternary Ammonium Support

Flood, Dillon T.,Asai, Shota,Zhang, Xuejing,Wang, Jie,Yoon, Leonard,Adams, Zo? C.,Dillingham, Blythe C.,Sanchez, Brittany B.,Vantourout, Julien C.,Flanagan, Mark E.,Piotrowski, David W.,Richardson, Paul,Green, Samantha A.,Shenvi, Ryan A.,Chen, Jason S.,Baran, Phil S.,Dawson, Philip E.

, p. 9998 - 10006 (2019)

DNA Encoded Libraries have proven immensely powerful tools for lead identification. The ability to screen billions of compounds at once has spurred increasing interest in DEL development and utilization. Although DEL provides access to libraries of unprec

Photoinduced Decarboxylative Phosphorothiolation of N-Hydroxyphthalimide Esters

Guo, Yu,Luo, Ying,Mu, Shiqiang,Xu, Jian,Song, Qiuling

supporting information, p. 6729 - 6734 (2021/09/11)

A visible-light-induced protocol for the synthesis of phosphorothioates is developed by employing the Ir-catalyzed decarboxylative phosphorothiolation of N-hydroxyphthalimide esters. This novel synthesis method utilizes carboxylic acids as raw material, which is stable, cheap, and commercially available. Scope studies show that this reaction has good compatibility of functional groups. Notably, both the synthesis of steric hindrance phosphorothioates and the later modification of some bioactive compounds are successfully achieved.

Photodecarboxylative Amination of Redox-Active Esters with Diazirines

Maharaj, Vishala,Chandrachud, Preeti P.,Che, Wen,Wojtas, Lukasz,Lopchuk, Justin M.

supporting information, p. 8838 - 8842 (2021/11/24)

Diazirines have been recently demonstrated to serve as electrophilic amination reagents that afford diaziridines, versatile heterocycles that are readily transformed into amines, hydrazines, and nitrogen-containing heterocycles. Here, we report the photodecarboxylative amination of redox-active esters with diazirines using inexpensive photoactivators under mild conditions with an enhanced scope for primary substrates. The stability of diazirines to blue light is demonstrated, paving the way for further research into other photochemical amination methods with these unique heterocycles.

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