84812-00-0

Basic information

• Product Name: 1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE
• Synonyms: 3,4-Dimethoxyphenyl beta-D-glucoside;3,4-DiMethoxyphenyl glucoside;(2S,3R,4S,5S,6R)-2-(3,4-DiMethoxyphenoxy)-6-(hydroxyMethyl)tetrahydro-2H-pyran-3,4,5-triol;1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE
• CAS NO: 84812-00-0
• Molecular Formula: C₁₄H₂₀O₈
• Molecular Weight: 316.304
• EINECS: 200-258-5
• Mol File: 84812-00-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE(84812-00-0)
• EPA Substance Registry System: 1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE(84812-00-0)

Safety Data

• Hazardous Substances Data: 84812-00-0(Hazardous Substances Data)

Usage

General Description

1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE is a chemical compound that consists of a phenyl group with two methoxy groups attached to it, along with a glucose molecule attached at the 4th position. 1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE is often used in pharmaceutical research and development due to its potential medicinal properties. It may have anti-inflammatory, antioxidant, or other therapeutic effects due to the presence of the phenyl and glucose moieties. It could also be used for its flavoring properties or as a fragrance in cosmetic products. Overall, 1,2-DINMETHOXY-PHENYL 4-O-BETA-D-GLUCOPYRANOSIDE has a wide range of potential applications in the fields of medicine, cosmetics, and flavoring.

Upstream product

• 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 
• 136112-50-0 2-Methoxyhydroquinone 4-O-<6-O-(4-O-α-L-rhamnopyranosyl)-syringyl>-β-D-glucopyranoside 

Relevant articles and documents

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.

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).