957753-00-3 Usage
Uses
Used in Luminescent Material Synthesis:
9-FluorenylMethylthiol is used as a precursor in the synthesis of luminophore materials for its ability to contribute to longer lifespans and more efficient luminescence. This makes it a valuable component in the development of advanced optical and electronic devices.
Used in Surface Self-Assembly:
9-FluorenylMethylthiol is used in surface self-assembly processes, particularly on gold surfaces, due to its self-assembly capabilities. This property allows for the creation of well-ordered and stable thin films, which can be utilized in various applications such as sensors, catalysts, and nanotechnology.
Used in Chiral Compounds:
The methylene group in 9-FluorenylMethylthiol provides a potential point of chirality, making it useful in the development of chiral compounds. Chiral compounds have applications in various fields, including pharmaceuticals, where they can be used to create enantiomerically pure drugs with specific therapeutic effects.
Check Digit Verification of cas no
The CAS Registry Mumber 957753-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,7,5 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 957753-00:
(8*9)+(7*5)+(6*7)+(5*7)+(4*5)+(3*3)+(2*0)+(1*0)=213
213 % 10 = 3
So 957753-00-3 is a valid CAS Registry Number.
957753-00-3Relevant academic research and scientific papers
NMR-based assignment of isoleucine: Vs. allo -isoleucine stereochemistry
Anderson, Zoe J.,Hobson, Christian,Needley, Rebecca,Song, Lijiang,Perryman, Michael S.,Kerby, Paul,Fox, David J.
, p. 9372 - 9378 (2017/11/22)
A simple 1H and 13C NMR spectrometric analysis is demonstrated that permits differentiation of isoleucine and allo-isoleucine residues by inspection of the chemical shift and coupling constants of the signals associated with the proton and carbon at the α-stereocentre. This is applied to the estimation of epimerisation during metal-free N-arylation and peptide coupling reactions.
Amino acid and peptide synthesis and functionalization by the reaction of thioacids with 2,4-dinitrobenzenesulfonamides
Crich, David,Sana, Kasinath,Guo, Songpo
, p. 4423 - 4426 (2008/03/12)
(Formula Presented) Readily prepared amino thioacids react at room temperature in DMF in the presence of cesium carbonate with 2,4- dinitrobenzenesulfonamides to give amides. When the sulfonamide is derived from an amino acid the method results in peptide bond formation, whereas the use of carbohydrate derived sulfonamides gives neoglycoconjugates.
