115654-61-0 Usage
Uses
Used in Medicinal Chemistry:
(S)-N-BOC-LEUCINE-NITRILE is used as a building block for the synthesis of pharmaceutical compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Drug Development:
In the pharmaceutical industry, (S)-N-BOC-LEUCINE-NITRILE is utilized as a key intermediate in the preparation of nitrogen-containing organic molecules, which are essential components in the creation of various medicinal agents.
Used in Organic Synthesis:
(S)-N-BOC-LEUCINE-NITRILE is employed as a protecting group in organic synthesis to temporarily mask reactive functional groups, facilitating controlled reactions and enhancing the yield of desired products.
Check Digit Verification of cas no
The CAS Registry Mumber 115654-61-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,6,5 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 115654-61:
(8*1)+(7*1)+(6*5)+(5*6)+(4*5)+(3*4)+(2*6)+(1*1)=120
120 % 10 = 0
So 115654-61-0 is a valid CAS Registry Number.
115654-61-0Relevant academic research and scientific papers
Photoinduced direct cyanation of C(sp3)-H bonds
Hoshikawa, Tamaki,Yoshioka, Shun,Kamijo, Shin,Inoue, Masayuki
, p. 874 - 887 (2013/05/09)
A general and practical synthetic protocol for the direct transformation of unreactive C(sp3)-H bonds to C(sp3)-CN bonds has been developed. The homolytic cleavage of the C-H bond is initiated by photo-excited benzophenone, and the resulting carbon radical subsequently reacts with tosyl cyanide to afford the corresponding nitrile in a highly efficient manner. The present methodology is widely applicable to various starting materials including ethers, alcohols, amine derivatives, alkanes, and alkylbenzenes. This newly developed C-H cyanation protocol provides a powerful tool for selective one-carbon elongation for the construction of architecturally complex molecules. Georg Thieme Verlag Stuttgart - New York.