63366-83-6

Basic information

• Product Name: ACETYL-TRANS-RESVERATROL
• Synonyms: ACETYL-TRANS-RESVERATROL;ACETIC ACID 4-[2-(3,5-DIACETOXY-PHENYL)-VINYL]-PHENYL ESTER
• CAS NO: 63366-83-6
• Molecular Formula: C₁₈H₁₈O₄
• Molecular Weight: 354.11
• Mol File: 63366-83-6.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 504.803 °C at 760 mmHg
• Flash Point: 221.436 °C
• Appearance: /
• Density: 1.241 g/cm³
• CAS DataBase Reference: ACETYL-TRANS-RESVERATROL(CAS DataBase Reference)
• NIST Chemistry Reference: ACETYL-TRANS-RESVERATROL(63366-83-6)
• EPA Substance Registry System: ACETYL-TRANS-RESVERATROL(63366-83-6)

Safety Data

• Hazardous Substances Data: 63366-83-6(Hazardous Substances Data)

Usage

General Description

ACETYL-TRANS-RESVERATROL is a modified form of the natural compound resveratrol, which is found in red wine, grapes, and certain other plants. It is believed to have antioxidant and anti-inflammatory properties, and has been studied for its potential health benefits. ACETYL-TRANS-RESVERATROL has been shown to have greater stability in the body and improved bioavailability compared to regular resveratrol, making it a promising compound for use in dietary supplements and pharmaceuticals. Some research suggests that ACETYL-TRANS-RESVERATROL may have potential in supporting cardiovascular health, protecting against age-related decline, and even inhibiting the growth of certain cancer cells. However, more studies are needed to fully understand its mechanisms and potential applications in medicine.

Upstream product

• 2628-16-2 p-acetoxystyrene 
• 25245-27-6 1-iodo-3,5-dimethoxybenzene 
• 192182-54-0 3,5-dimethoxyphenylboronic acid 
• 123-08-0 4-hydroxy-benzaldehyde 
• 878-00-2 4-formylphenyl acetate 
• 1532557-35-9 2-[(3,5-dimethoxybenzyl)sulfonyl]-1,3-benzothiazole 
• 1532557-34-8 2-[(3,5-dimethoxybenzyl)sulfanyl]-1,3-benzothiazole 
• 705-76-0 3,5-dimethoxybenzyl alcohol 
• 156-38-7 4-hydroxyphenylacetate 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 1110615-49-0 C₁₉H₁₈O₆ 
• 33527-94-5 4-acetoxyiodobenzene 
• 40243-87-6 3,5-dimethoxystyrene 
• 72470-95-2 3,5-dimethoxybenzenediazonium tetrafluoroborate 

Downstream Products

• 411233-11-9 4'-Acetylresveratrol 
• 537-42-8 3,5-dimethoxy-4'-hydroxy-trans-stilbene 
• 116518-94-6 3,5-di-O-methyldihydroresveratrol 

Relevant articles and documents

Novel Carbazole-Based N-Heterocyclic Carbene Ligands to Access Synthetically Relevant Stilbenes in Pd-Catalyzed Coupling Processes

A series of new carbazole-based N-heterocyclic carbene (NHC) ligands have been synthesized in a simple and facile synthetic route and subsequently used in a Pd/carbazole-based NHC catalytic system, which was found to be effective in catalyzing Heck reactions to provide substituted stilbene derivatives in good yields. Several bioactive stilbenes, including pterostilbene, pinosylvin, trimethoxy resveratrol, and resveratrol, were synthesized in good yields, and a 10 mmol scale-up was also performed for trimethoxy resveratrol. The synthetic application was also extended by performing a double-tandem chemoselective Heck reaction followed by Miyaura borylation in a one-pot procedure to give single-step access to synthetically useful stilbenyl boronate esters. Similarly, a unique triple-tandem protocol of a chemoselective Heck reaction/Miyaura borylation/Suzuki–Miyaura coupling reaction sequence was performed for the one-pot modification of biologically relevant molecules.

POLYMER-SUPPORTED TRANSITION CATALYST

A long life catalyst is provided that is conveniently and inexpensively capable of being produced and that is highly active and has inhibited metal leakage. According to aspects of the present invention, a catalyst is provided that includes: a polymer including a plurality of first structural units and a plurality of second structural units; and metal acting as a catalytic center, wherein at least part of the metal is covered with the polymer, each of the plurality of first structural units has a first atom constituting a main chain of the polymer and a first substituent group bonded to the first atom, a second atom included in each of the plurality of second structural units is bonded to the first atom, and the second atom is different from the first atom, or at least one of all substituent groups on the second atom is different from the first substituent group.

Synthesis of pterostilbene by julia olefination

A simple, E-stereoselective route for the synthesis of the biologically active compounds trans-pterostilbene and tetramethoxy stilbene from the readily available starting materials 3,5-dimethoxy benzyl alcohol and 4-hydroxy benzaldehyde was developed using Julia olefination as a key reaction. Taylor & Francis Group, LLC.