198545-20-9 Usage
Description
FMOC-D-ORN(MTT)-OH, also known as N-(9-fluorenylmethoxycarbonyl)-D-ornithine (MTT), is an amino acid derivative that plays a significant role in chemical synthesis and peptide chemistry. It is characterized by its white to off-white crystalline appearance and is widely utilized in various applications across different industries due to its unique chemical properties.
Uses
Used in Chemical Synthesis:
FMOC-D-ORN(MTT)-OH is used as a building block for the synthesis of various complex organic molecules. Its application in this field is primarily due to its ability to facilitate the formation of amide bonds, which are crucial in the construction of peptides and other biomolecules.
Used in Peptide Chemistry:
In peptide chemistry, FMOC-D-ORN(MTT)-OH is employed as a protected amino acid, which is essential for the stepwise synthesis of peptides. The protection of the amino group by the 9-fluorenylmethoxycarbonyl (Fmoc) group allows for selective deprotection and coupling reactions, enabling the controlled assembly of peptide sequences.
Used in Pharmaceutical Industry:
FMOC-D-ORN(MTT)-OH is used as a key intermediate in the development of novel pharmaceutical compounds. Its application in this industry is driven by its potential to contribute to the design and synthesis of new drugs with improved therapeutic properties.
Used in Research and Development:
In the field of research and development, FMOC-D-ORN(MTT)-OH is utilized as a valuable tool for studying the structure, function, and interactions of peptides and proteins. Its use in this context aids in advancing our understanding of various biological processes and the development of targeted therapeutic strategies.
Used in Analytical Chemistry:
FMOC-D-ORN(MTT)-OH is employed as a reagent in various analytical techniques, such as high-performance liquid chromatography (HPLC) and mass spectrometry (MS), for the detection and quantification of peptides and proteins. Its application in this field is attributed to its ability to enhance the detection and separation of these biomolecules.
Check Digit Verification of cas no
The CAS Registry Mumber 198545-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,5,4 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 198545-20:
(8*1)+(7*9)+(6*8)+(5*5)+(4*4)+(3*5)+(2*2)+(1*0)=179
179 % 10 = 9
So 198545-20-9 is a valid CAS Registry Number.