63503-05-9 Usage
Uses
Used in Chemical Synthesis:
2-NAPHTHYL-ALPHA-L-FUCOPYRANOSIDE is used as an intermediate in the synthesis of various complex organic compounds, particularly those involving the fucopyranose moiety. Its unique structure allows for selective functionalization and modification, making it a valuable building block in organic chemistry.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-NAPHTHYL-ALPHA-L-FUCOPYRANOSIDE is used as a research tool for studying the interactions of fucopyranose-containing molecules with biological targets. Its 2-naphthyl group provides a convenient handle for monitoring these interactions through various analytical techniques, such as fluorescence spectroscopy and nuclear magnetic resonance (NMR) spectroscopy.
Used in Glycobiology:
2-NAPHTHYL-ALPHA-L-FUCOPYRANOSIDE is employed in the field of glycobiology as a probe to investigate the role of fucopyranose-containing carbohydrates in cellular processes and molecular recognition. Its distinctive structure allows researchers to gain insights into the specific roles of fucopyranose residues in various biological systems.
Used in Analytical Chemistry:
As an analytical standard, 2-NAPHTHYL-ALPHA-L-FUCOPYRANOSIDE is used to calibrate and validate analytical instruments and methods that are designed to detect and quantify fucopyranose-containing compounds. Its well-defined structure and spectral properties make it an ideal reference material for these purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 63503-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,0 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63503-05:
(7*6)+(6*3)+(5*5)+(4*0)+(3*3)+(2*0)+(1*5)=99
99 % 10 = 9
So 63503-05-9 is a valid CAS Registry Number.
63503-05-9Relevant academic research and scientific papers
Synthesis of aryl α-O-L-rhamnopyranoside by two-step reaction in one pot
Liu, Nianping,Tian, Xiangguang,Ding, Zekun,Zhou, Yongda,Zhang, Wan,Wang, Qingbing,Zhang, Yi,Gu, Yijun,Zhang, Jianbo
, p. 220 - 234 (2017/11/10)
The title compounds were conveniently synthesized by a phase transfer catalyzed approach in two steps and one pot using the rhamnopyranosyl chloride as key intermediate. The twostep one-pot procedure is more convenient and environmentally friendly, compared to the published synthetic routes. Besides, the structure-reactivity relationship and the plausible mechanism for this base-catalyzed glycosylation were discussed bymeans of the Hammett equation.
On the regioselectivity of the protease subtilisin towards the acylation of enantiomeric pairs of benzyl and naphthyl glycopyranosides. Part 2
Danieli, Bruno,Peri, Francesco,Roda, Gabriella,Carrea, Giacomo,Riva, Sergio
, p. 2045 - 2060 (2007/10/03)
Subtilisin-catalyzed esterification of several enatiomeric benzyl and naphthyl glycopyranosides has been investigated. The D-sugar derivatives were all good substrates and subtilisin regioselectivity was similar with all the compounds tested, the 3-OH being acylated predominantly. On the other hand, most of the L-glycopyranosides were transformed during longer reaction times with a lower regioselectivity, the 2-OH being preferentially but not exclusively acylated.
