139726-40-2 Usage
Uses
Used in Pharmaceutical Industry:
See R-D-Glucopyranoside, α-D-fructofuranosyl, esters, 6-[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)2-propenoate] is used as a potential pharmaceutical agent for its possible biological activity, which may be harnessed for the development of new drugs or therapies. See R-D-Glucopyranoside,â-D-fructofuranosyl,esters,6-[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)2-propenoate] 's unique structure could allow it to interact with biological targets in novel ways, offering new avenues for treatment.
Used in Food Industry:
In the food industry, See R-D-Glucopyranoside, α-D-fructofuranosyl, esters, 6-[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)2-propenoate] may be utilized as a functional ingredient or additive, capitalizing on its structural properties to enhance food products' taste, texture, or shelf life.
Used in Cosmetic Industry:
See R-D-Glucopyranoside, α-D-fructofuranosyl, esters, 6-[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)2-propenoate] is used as an ingredient in cosmetic products for its potential to provide skincare benefits, such as antioxidant properties or moisturizing effects, due to the presence of hydroxy and dimethoxy groups in its structure.
Further research is necessary to fully understand the properties and potential uses of See R-D-Glucopyranoside, α-D-fructofuranosyl, esters, 6-[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)2-propenoate], as its complex structure and possible biological activity suggest a wide range of applications across different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 139726-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,7,2 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 139726-40:
(8*1)+(7*3)+(6*9)+(5*7)+(4*2)+(3*6)+(2*4)+(1*0)=152
152 % 10 = 2
So 139726-40-2 is a valid CAS Registry Number.
139726-40-2Relevant academic research and scientific papers
PHENYLPROPANOID SACCHARIDE ESTERS, METHODS AND USES THEREOF
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Paragraph 00062; 00072, (2020/09/27)
The present disclosure relates to phenylpropanoid saccharide esters, methods for the synthesis of libraries of phenylpropanoid saccharide esters with different degree and place of substitution in the sugar core, and their use as antimicrobial agents, cytotoxic agents and/or antitumoral agents. The present disclosure relates to a compound for formula I wherein R1, R2, R3 and R4 are independently selected from each other; R1 is selected from H or COCH3, R2, R3 and R4 is selected from H, OCH3, OH, for use in a method for the treatment of a microbial infection, or for use in a method for the treatment of a fungal infection or for use in a method for the treatment of cancer.
Four new phenolic glycosides from Polygala tenuifolia
Ikeya,Sugama,Okada,Mitsuhashi
, p. 2600 - 2605 (2007/10/02)
Four new phenolic glycosides, tenuifolisides A (1), B (2), C (3), and D (4) together with a known phenolic glycoside, β-D-(3-O-sinapoyl)-fructofuranosyl-α-D-(6-O-sinapoyl)-glucopyranoside (5) were isolated from the roots of Polygala tenuifolia. The structures of these new compounds were characterized as β-D-[3-O-(3,4,5-trimethoxycinnamoyl)]fructofuranosyl-α-D-[6-O-(p-hydr oxybenzoyl)]-glucopyranoside (1), β-D-(3-O-sinapoyl)-fructofuranosyl-α-D-[6-O-(p-hydroxybenzoyl)]-gluco pyranoside (2), β-D-[3-O-(3,4,5-trimethoxycinnamoyl)]-fructofuranosyl-α-D-(6-O-sinapo yl)glucopyranoside (3), and 1,5-anhydro-[6-O-(3,4,5-trimethoxycinnamoyl)]-D-glucitol (4), respectively, on the basis of chemical and spectral evidence including two dimensional nuclear magnetic resonance (2D-NMR) studies.
