59587-94-9 Usage
Uses
Used in Pharmaceutical Research:
BOC-GLU-PHENYL ESTER is used as a building block for the synthesis of small molecules, contributing to the development of new pharmaceutical compounds. Its presence in the synthesis process aids in the creation of diverse molecular structures with potential therapeutic applications.
Used in Peptide Synthesis:
BOC-GLU-PHENYL ESTER is used as a component in peptide synthesis, facilitating the formation of peptide bonds and contributing to the production of bioactive peptides. Its role in this process is crucial for the development of peptide-based drugs and therapeutic agents.
Used in Drug Delivery Systems:
BOC-GLU-PHENYL ESTER is employed in drug delivery systems to enhance the efficiency and targeting of pharmaceutical compounds. Its compatibility with various synthetic techniques allows for the development of innovative drug delivery platforms, improving the bioavailability and therapeutic outcomes of drugs.
Used in Chemical Research:
BOC-GLU-PHENYL ESTER is utilized as a research tool in chemical research, providing insights into the properties and behavior of ester derivatives and their interactions with other molecules. Its stability and compatibility with analytical techniques make it an essential component in the study of chemical reactions and mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 59587-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,8 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59587-94:
(7*5)+(6*9)+(5*5)+(4*8)+(3*7)+(2*9)+(1*4)=189
189 % 10 = 9
So 59587-94-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H21NO6/c1-16(2,3)23-15(21)17-12(9-10-13(18)19)14(20)22-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,18,19)/t12-/m0/s1
59587-94-9Relevant academic research and scientific papers
A Convenient Asymmetric Synthesis of Thalidomide
Robin, Sylvie,Zhu, Jiarong,Galons, Herve,Pham-Huy, Chuong,Claude, Jean Roger,et al.
, p. 1249 - 1252 (2007/10/02)
Benzyloxyamine reacted with BOC-glutamic-α-phenyl ester in the presence of carbodiimide to give BOC-amino-N-benzyloxypiperidinedione.Deprotection of the amino group followed by phthaloylation led to N-benzyloxythalidomide which was then converted into thalidomide.
