84812-00-0

Usage

Uses

Used in Pharmaceutical Research and Development:
1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE is used as a pharmaceutical compound for its potential medicinal properties, such as anti-inflammatory and antioxidant effects. The presence of the phenyl and glucose moieties contributes to its therapeutic potential.
Used in Cosmetic Products:
In the cosmetic industry, 1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE is used as a fragrance ingredient due to its pleasant scent. Its incorporation into cosmetic products can enhance the sensory experience for consumers.
Used in Flavoring Industry:
1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE is used as a flavoring agent in the food and beverage industry. Its unique taste profile can add depth and complexity to various products, enhancing the overall flavor experience.
Overall, 1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE has a wide range of potential applications across the fields of medicine, cosmetics, and flavoring, making it a valuable compound for research and development.

Upstream product

• 136112-50-0 2-Methoxyhydroquinone 4-O-<6-O-(4-O-α-L-rhamnopyranosyl)-syringyl>-β-D-glucopyranoside 
• 83-87-4 D-glucose pentaacetate 
• 136112-51-1 Acetic acid (2R,3R,4S,5R,6S)-3,5-diacetoxy-2-acetoxymethyl-6-(3,4-dimethoxy-phenoxy)-tetrahydro-pyran-4-yl ester 
• 2033-89-8 3,4-dimethoxyphenol 
• 74808-10-9 2,3,4,6-tetra-O-acetyl-d-glucopyranosyl trichloroacetimidate 
• 186581-53-3 diazomethane 
• 109194-60-7 tachioside 

Relevant academic research and scientific papers

Preparation method of antitumor active compound

The invention relates to a preparation method of antitumor active compound, belonging to the field of medicinal chemistry. The method comprises the steps of enabling commercialized fully-acetylated glucose serving as a starting raw material and methylene dichloride serving as a solvent to react with 3, 4-dimethoxyphenol under the catalytic action of boron trifluoride ether so as to form a glucose anomeric carbon position-substituted glycoside intermediate; then, removing acetyl under the alkaline condition of sodium methylate, and enabling the product to have a regioselective chemical reaction with benzoyl chloride prepared by using full benzyl-protected anhydrous gallic acid so as to obtain a key glycosyl intermediate; finally, carrying out palladium-carbon reduction to remove benzyl protection. The glycoside natural product 1 is formed in high yield by means of simple and efficient reactions in the four steps; the prepared glycoside natural product has good tumor cytotoxic activity. The structural formula of the glycoside natural product 1 is described in the description.

Synthesis of tyrosyl-DNA phosphodiesterase i inhibitors

The first report for the synthesis of tyrosyl-DNA phosphodiesterase I inhibitors 3,4-dimethoxyphenol-1-β-d-(6′-O-galloyl)glucopyranoside 3 and 3-(4-hydroxy-3-methoxyphenyl)propane-1,2-diol 2-β-d-(6′-O-galloyl) glucopyranoside 5 has been accomplished starting from readily available d-glucose as a starting material. An efficient and general approach has been reported for the synthesis of compounds 3 and 5 with an overall yield of 26% and 27%, respectively.

Studies on the constituents of the bark of Kalopanax pictus Nakai

Five new compounds, kalopanaxsaponin G (2) and kalopanaxins A (6), B (8), C (11) and D (13), were isolated from the bark of Kalopanax pictus together with nine known compounds, kalopanaxsaponins A (1) and B (5), pericarpsaponin P(J3) (3), hederasaponin B (4), syringin (7), protocatechuic acid (9), coniferin (10), liriodendrin (=dl-syringaresinol di-O-glucopyranoside) (12), glucosyringic acid (14) and chlorogenic acid (15). The structures of the new compounds were characterized as hederagenin 28-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6)-β-D- glucopyranoside (2), ferulylaldehyde (=coniferylaldehyde) 4-O-β-D-glucopyranoside (6), coniferin 6'-O-(4-O-α-L-rhamnopyranosyl)-syringate (8), 2-methoxyhydroquinone 4-O-[6-O[(4-O-α-L-rhamnopyranosyl)-syringyl]-β-D-glucopyranoside (11) and coniferyl alcohol 4-O-β-D-apiofuranosyl(1→2)-β-D-glucopyranoside (=coniferin 2'-O-β-D-apiofuranoside) (13).