155905-78-5 Usage
Description
Boc-D-Cyclobutylglycine, a chemical compound with the molecular formula C14H23NO4, is a derivative of cyclobutylglycine, an amino acid not found naturally in proteins. It is a Boc-protected amino acid, where the amino group is protected by a Boc (tert-butoxycarbonyl) group to prevent unwanted reactions during the synthesis process. Boc-D-Cyclobutylglycine is commonly used in the synthesis of peptides and other organic compounds, serving as a building block in the preparation of pharmaceuticals and agrochemicals. Its potential applications in drug discovery and development are attributed to its ability to mimic naturally occurring amino acids in peptide molecules.
Uses
Used in Pharmaceutical Industry:
Boc-D-Cyclobutylglycine is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its ability to mimic naturally occurring amino acids in peptide molecules allows for the creation of novel peptide-based drugs with improved properties and therapeutic effects.
Used in Agrochemical Industry:
Boc-D-Cyclobutylglycine is used as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds, leading to increased crop yields and agricultural productivity.
Used in Peptide Synthesis:
Boc-D-Cyclobutylglycine is used as a protected amino acid in peptide synthesis, allowing for the stepwise assembly of peptide chains with controlled selectivity and minimized side reactions. The Boc protection group can be selectively removed during the synthesis process, enabling the incorporation of Boc-D-Cyclobutylglycine into longer peptide sequences.
Used in Organic Synthesis:
Boc-D-Cyclobutylglycine is used as a versatile building block in the synthesis of various organic compounds, including natural products, pharmaceutical intermediates, and specialty chemicals. Its unique structure and reactivity make it a valuable component in the development of novel organic molecules with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 155905-78-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,9,0 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155905-78:
(8*1)+(7*5)+(6*5)+(5*9)+(4*0)+(3*5)+(2*7)+(1*8)=155
155 % 10 = 5
So 155905-78-5 is a valid CAS Registry Number.
155905-78-5Relevant articles and documents
A Versatile Method for the Synthesis of (S)- or (R)-Cycloalkylglycines, (S)- or (R)-N-Heterocyclic and α,β-Unsaturated N-Heterocyclic α-Amino Acids
Pauly, Regine,Sasaki, N. Andre,Potier, Pierre
, p. 237 - 240 (2007/10/02)
Two different types of cyclic α-amino acids, cycloalkylglycines and N-heterocyclic α-amino acids, were prepared in optically pure form from the same chiral synthon 1-(R) (or 1-(S)) simply by altering the quantity or type of base required for anion formation.Elaboration of the heterocyclic intermediate 3 provided α,β-unsaturated N-heterocyclic α-amino acids.
