153815-60-2 Usage
General Description
FMOC-L-TRYPTOPHANOL, also known as Fmoc-Trp-OH, is a derivative of the essential amino acid Tryptophan, commonly used in the field of biochemistry, particularly in peptide synthesis. It is recognized for its role in the procedure known as Fluorenylmethyloxycarbonyl (Fmoc) protection, used to prevent side reactions during the synthesis process. FMOC-L-TRYPTOPHANOL is designed for laboratory use and is often used in drugs and pharmaceuticals. It has a complex structure, including a benzyl alcohol group and is characterized by its light sensitivity. As such, it requires careful handling and storage, typically in cool and dark conditions, to maintain its stability and effectiveness.
Check Digit Verification of cas no
The CAS Registry Mumber 153815-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,8,1 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 153815-60:
(8*1)+(7*5)+(6*3)+(5*8)+(4*1)+(3*5)+(2*6)+(1*0)=132
132 % 10 = 2
So 153815-60-2 is a valid CAS Registry Number.
153815-60-2Relevant articles and documents
Design, synthesis, and immunochemical characterization of a chimeric glycopeptide corresponding to the Shigella flexneri Y O-polysaccharide and its peptide mimic MDWNMHAA
Hossany, B. Rehana,Johnston, Blair D.,Wen, Xin,Borrelli, Silvia,Yuan, Yue,Johnson, Margaret A.,Pinto, B. Mario
experimental part, p. 1412 - 1427 (2009/12/05)
Two glycopeptide chimeras corresponding to the Shigella flexneri Y O-polysaccharide and its peptide mimic were designed in an attempt to improve the binding affinity by increasing the entropy of binding relative to the original octapeptide mimic of the O-
Synthesis of Chiral N-Protected β-Amino Alcohols by the Use of UNCAs
Fehrentz, Jean-Alain,Califano, Jean-Christophe,Amblard, Muriel,Loffet, Albert,Martinez, Jean
, p. 569 - 572 (2007/10/02)
A facile synthesis of a wide variety of N-protected β-amino alcohol derivatives under mild conditions is described.N-urethane protected amino acid N-carboxyanhydrides (UNCAs) were used as starting material and reduced into the corresponding alcohols with
