82911-71-5 Usage
Uses
Used in Peptide Synthesis:
FMOC-OBt is used as a protecting agent for the synthesis of complex glycopeptides and O-phosphotyrosine analogs. It plays a crucial role in protecting specific functional groups during the synthesis process, allowing for the selective formation of desired peptide bonds and facilitating the synthesis of complex peptide structures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, FMOC-OBt is used as a protecting agent for the synthesis of therapeutic peptides and glycopeptides. Its ability to protect specific functional groups during the synthesis process enables the development of novel and effective drug candidates with improved pharmacological properties.
Used in Research and Development:
FMOC-OBt is also used in research and development for the synthesis of various peptides and glycopeptides. It is an essential tool for scientists working on the discovery and development of new therapeutic agents, as well as for understanding the structure and function of biologically active peptides.
Check Digit Verification of cas no
The CAS Registry Mumber 82911-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,1 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82911-71:
(7*8)+(6*2)+(5*9)+(4*1)+(3*1)+(2*7)+(1*1)=135
135 % 10 = 5
So 82911-71-5 is a valid CAS Registry Number.
InChI:InChI=1/C21H15N3O3/c25-21(27-24-20-12-6-5-11-19(20)22-23-24)26-13-18-16-9-3-1-7-14(16)15-8-2-4-10-17(15)18/h1-12,18H,13H2
82911-71-5Relevant articles and documents
An improved synthesis of a fluorescent gabapentin-choline conjugate for single molecule detection
Wu, Haitao,Kaur, Gurpreet,Griffiths, Gary L.
supporting information; experimental part, p. 2100 - 2102 (2009/07/19)
Voltage-gated calcium ion channels comprise pore-forming α1 and auxiliary α2δ, β, and γ subunits. They are important molecular devices involved in a variety of cell functions. Fluorescently labeled acylcholine analogues are important
Introduction of 9-fluorenylmethyloxycarbonyl, trichloroethoxycarbonyl, and benzyloxycarbonyl amine protecting groups into O-unprotected hydroxyamino acids using succinimidyl carbonates
Paquet, Alenka
, p. 976 - 980 (2007/10/02)
9-Fluorenylmethyl succinimidyl, pentachlorophenyl, and benzotriazole-1-yl carbonates were prepared and their reactivity with L-serine and L-serine benzyl ester was compared.The most efficient reagent, 9-fluorenylmethyl succinimidyl carbonate, was used for the preparation of 9-flourenylmethyloxycarbonyl derivatives of other hydroxyamino acids and hydroxyamino acid esters in high yields.The use of trichloroethyl and benzyl succinimidyl carbonates for an efficient conversion of hydroxyamino acids and their esters into the corresponding N-trichloroethoxycarbonyl and benzyloxycarbonyl derivatives is described.
