61548-34-3 Usage
Uses
Used in Pharmaceutical Industry:
â-D-Glucopyranoside,2-(3,4-dihydroxyphenyl)ethyl 3-O-(6-deoxy-R-L-mannopyranosyl)is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure allows it to interact with biological systems, making it a candidate for the development of new drugs and therapies.
Used in Food Industry:
In the food industry, â-D-Glucopyranoside,2-(3,4-dihydroxyphenyl)ethyl 3-O-(6-deoxy-R-L-mannopyranosyl)can be used as a natural sweetener or flavor enhancer due to its sugar-based structure. Its presence in natural products also suggests that it may have potential applications in the development of novel food products with unique taste profiles.
Used in Cosmetic Industry:
â-D-Glucopyranoside,2-(3,4-dihydroxyphenyl)ethyl 3-O-(6-deoxy-R-L-mannopyranosyl)can be utilized in the cosmetic industry for its potential skin-friendly properties. â-D-Glucopyranoside,2-(3,4-dihydroxyphenyl)ethyl 3-O-(6-deoxy-R-L-mannopyranosyl)'s ability to interact with biological systems may provide benefits such as moisturization, skin protection, or even anti-aging effects.
Used in Research:
â-D-Glucopyranoside,2-(3,4-dihydroxyphenyl)ethyl 3-O-(6-deoxy-R-L-mannopyranosyl)is also used in research settings to study the interactions between carbohydrates and biological systems. Its unique structure and potential biological activities make it an interesting subject for scientific investigation, which could lead to new discoveries and applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 61548-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,4 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61548-34:
(7*6)+(6*1)+(5*5)+(4*4)+(3*8)+(2*3)+(1*4)=123
123 % 10 = 3
So 61548-34-3 is a valid CAS Registry Number.
61548-34-3Relevant academic research and scientific papers
He, Zheng-Dan,Ueda, Shinichi,Akaji, Masako,Fujita, Tetsuro,Inoue, Kenichiro,Yang, Chong-Ren
, p. 709 - 716 (1994)
Two new phenylethanoid glycosides, lipedosides A-I and A-II as well six new monoterpene glycosides, lipedosides B-I-B-IV were isolated together with three known constituents, osmanthuside B, anatolioside and linalool from Ligustrum pedunculare.Their structures have been elucidated by chemical and spectroscopic methods.
Collective syntheses of phenylethanoid glycosides by interrupted Pummerer reaction mediated glycosylations
Zhao, Yueqi,Zeng, Jing,Liu, Yan,Xiao, Xiong,Sun, Guangfei,Sun, Jiuchang,Shu, Penghua,Fu, Dengxian,Meng, Lingkui,Wan, Qian
, p. 471 - 497 (2019/04/10)
The collective total syntheses of nine natural phenylethanoid glycosides (PhEGs) together with proposed Incanoside B in a divergent mode were described. By using a core disaccharide as common intermediate, our developed interrupted Pummerer reaction media
Verbascoside and Isoverbascoside from Paulownia Tomentosa Steud
Schilling, Gerhard,Huegel, Michael,Mayer, Walter
, p. 1633 - 1635 (2007/10/02)
The structure of verbascoside and isoverbascoside, isolated from the leaves of Paulownia tomentosa Steud. have been determined by NMR spectroscopy and partially hydrolysis to be β-(3,4-dihydroxyphenyl)ethyl-O-α-1-rhamnosyl(1-->3)-β-D-(4-O-caffeoyl)-glucopyranoside (1) and β-(3,4-dihydroxyphenyl)ethyl-O-α-L-rhamnosyl(1-->3)-β-D-(6-O-caffeoyl)-glucopyranoside (2). - Key words: Paulownia tomentosa Steud., Caffeoylglycoside, Verbascoside
