132388-64-8 Usage
Description
FMOC-ASN(TRT)-OPFP is a chemical compound that is used in various applications across different industries. It is a derivative of FMOC-protected amino acids, which are commonly used in peptide synthesis. FMOC-ASN(TRT)-OPFP is characterized by its unique structure and properties, making it a valuable component in various applications.
Uses
Used in Pharmaceutical Industry:
FMOC-ASN(TRT)-OPFP is used as a building block in the synthesis of peptides and proteins for pharmaceutical applications. Its FMOC protection allows for selective deprotection and coupling reactions, enabling the efficient synthesis of complex peptide structures.
Used in Chemical Research:
FMOC-ASN(TRT)-OPFP is used as a research tool in the development of new chemical compounds and materials. Its unique structure and properties make it a valuable component in the synthesis of novel molecules with potential applications in various fields.
Used in Biochemical Applications:
FMOC-ASN(TRT)-OPFP is used in biochemical research to study the structure and function of proteins and peptides. Its FMOC protection allows for the controlled synthesis and modification of biomolecules, enabling researchers to investigate their properties and potential applications.
Used in Analytical Chemistry:
FMOC-ASN(TRT)-OPFP is used as a reagent in analytical chemistry for the detection and quantification of specific compounds. Its unique structure and properties make it a valuable tool in the development of new analytical methods and techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 132388-64-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,8 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132388-64:
(8*1)+(7*3)+(6*2)+(5*3)+(4*8)+(3*8)+(2*6)+(1*4)=128
128 % 10 = 8
So 132388-64-8 is a valid CAS Registry Number.
InChI:InChI=1/C44H31F5N2O5/c45-36-37(46)39(48)41(40(49)38(36)47)56-42(52)35(51-43(53)55-24-34-32-22-12-10-20-30(32)31-21-11-13-23-33(31)34)25-54-26-50-44(27-14-4-1-5-15-27,28-16-6-2-7-17-28)29-18-8-3-9-19-29/h1-23,26,34-35H,24-25H2,(H,51,53)/t35-/m0/s1
132388-64-8Relevant articles and documents
Protection of carboxamide functions by the trityl residue. Application to peptide synthesis
Sieber,Riniker
, p. 739 - 742 (2007/10/02)
Carboxamide functions may be tritylated by an acid-catalyzed reaction with triphenylmethanol and acetic anhydride in glacial acetic acid. The ω-trityl group of asparagine and glutamine is cleavable by TFA, but stable to strong mineral acids in aqueous solution, as well as to nucleophiles and bases. In peptide syntheses, it is ideally suited for combination with side-chain protections of the t.butyl-type.
