65420-40-8 Usage
Description
N-Boc-N'-xanthyl-L-asparagine, also known as Boc-Asn(Xan)-OH, is an asparagine derivative characterized by the presence of a Boc protecting group and a xanthyl moiety attached to the nitrogen atoms. This unique structure allows it to be used in various chemical synthesis and biology studies, making it a valuable compound for research purposes.
Uses
Used in Chemical Synthesis:
N-Boc-N'-xanthyl-L-asparagine is used as a building block in the synthesis of complex organic molecules and pharmaceutical compounds. Its Boc protecting group can be selectively removed under mild conditions, facilitating the incorporation of the asparagine moiety into larger molecules.
Used in Biology Studies:
In biological research, N-Boc-N'-xanthyl-L-asparagine serves as a valuable tool for studying protein synthesis, enzyme activity, and other biological processes. The xanthyl moiety attached to the molecule can be used for fluorescence-based assays, allowing researchers to monitor the behavior of the compound within biological systems.
Used in Peptide Synthesis:
N-Boc-N'-xanthyl-L-asparagine is used as a protected amino acid in the synthesis of peptides and peptide-based drugs. The Boc protecting group ensures that the asparagine side chain remains unreactive during the coupling steps of peptide synthesis, preventing unwanted side reactions and improving the overall yield of the desired peptide product.
Used in Drug Development:
In the pharmaceutical industry, N-Boc-N'-xanthyl-L-asparagine can be used as a starting material for the development of new drugs targeting various diseases. Its unique structure and functional groups can be exploited to design molecules with specific biological activities, potentially leading to the discovery of novel therapeutic agents.
Overall, N-Boc-N'-xanthyl-L-asparagine is a versatile compound with a wide range of applications in chemical synthesis, biology studies, peptide synthesis, and drug development. Its unique structure and functional groups make it an invaluable tool for researchers and scientists working in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 65420-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,2 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65420-40:
(7*6)+(6*5)+(5*4)+(4*2)+(3*0)+(2*4)+(1*0)=108
108 % 10 = 8
So 65420-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C22H24N2O6/c1-22(2,3)30-21(28)23-15(20(26)27)12-18(25)24-19-13-8-4-6-10-16(13)29-17-11-7-5-9-14(17)19/h4-11,15,19H,12H2,1-3H3,(H,23,28)(H,24,25)(H,26,27)/t15-/m0/s1
65420-40-8Relevant articles and documents
Peptide Synthesis. Part 3. Comparative Solid-phase Syntheses of Human β-Endorphin on Polyamide Supports using t-Butoxycarbonyl and Fluorenylmethoxycarbonyl Protecting Groups
Atherton, Eric,Caviezel, Mario,Fox, Hazel,Harkiss, Diana,Over, Hilary,Sheppard, Robert C.
, p. 65 - 73 (2007/10/02)
Solid-phase syntheses of the 31 residue peptide human β-endorphin on polar polyamide supports are described.Minimisation of acidic reaction conditions by replacement of the customary t-butoxycarbonyl and benzyl-based protecting groups by fluorenylmethoxyc
