22223-38-7 Usage
Uses
Used in Pharmaceutical Synthesis:
N-(ethoxycarbonyl)tryptophan is used as a building block for the synthesis of pharmaceuticals, providing a versatile and reactive intermediate for the development of new drugs.
Used in Biochemical Research:
N-(ethoxycarbonyl)tryptophan is used as a tool to investigate the structure and function of specific proteins and enzymes, contributing to a better understanding of biological processes and the development of targeted therapies.
Used in Peptide and Protein Synthesis:
N-(ethoxycarbonyl)tryptophan is used as an intermediate in the synthesis of peptides and proteins, enabling the creation of complex biological molecules for research and therapeutic applications.
Used in Organic Chemistry:
N-(ethoxycarbonyl)tryptophan is used in various chemical reactions due to its unique chemical properties, making it a valuable tool for the development of new chemical compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 22223-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,2 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22223-38:
(7*2)+(6*2)+(5*2)+(4*2)+(3*3)+(2*3)+(1*8)=67
67 % 10 = 7
So 22223-38-7 is a valid CAS Registry Number.
22223-38-7Relevant academic research and scientific papers
Organocatalytic Enantioselective Addition of α-Aminoalkyl Radicals to Isoquinolines
Liu, Xiangyuan,Liu, Yang,Chai, Guobi,Qiao, Baokun,Zhao, Xiaowei,Jiang, Zhiyong
supporting information, p. 6298 - 6301 (2018/10/09)
With a dual organocatalytic system involving a chiral phosphoric acid and a dicyanopyrazine-derived chromophore (DPZ) photosensitizer and under the irradiation with visible light, an enantioselective Minisci-type addition of α-amino acid-derived redox-active esters (RAEs) to isoquinolines has been developed. A variety of prochiral α-aminoalkyl radicals generated from RAEs were successfully introduced on isoquinolines, providing a range of valuable α-isoquinoline-substituted chiral secondary amines in high yields with good to excellent enantioselectivities.
