143207-58-3 Usage
Chemical Class
Polyphenols
Appearance
Crystalline solid
Solubility
Soluble in ethanol, methanol, and acetone; slightly soluble in water
Natural Sources
Red wine, grapes, peanuts, and some berries
Antioxidant Properties
Resveratrol is a potent antioxidant, which helps neutralize harmful free radicals in the body
Anti-Inflammatory
May help reduce inflammation in the body
Cardiovascular Protection
Potentially protects against heart disease
Anti-Aging
May slow down the aging process
Anti-Cancer
Studied for its potential effects against cancer
Therapeutic Applications
Widely researched for its potential use in various fields of medicine
Safety
Generally considered safe for consumption in moderate amounts, but excessive intake may cause side effects such as diarrhea and nausea
Synonyms
Trans-resveratrol, 3,5,4'-trihydroxy-trans-stilbene, and (E)-3-(4-hydroxystyryl)phenol
Molecular Weight
228.24 g/mol
Chemical Structure
A stilbene derivative with two hydroxyl groups at the 1,2-positions of a benzene ring and a phenyl group attached to the 3-position
Melting Point
254-256°C (489.2-491.6°F)
Boiling Point
Not well-defined due to its solid state at room temperature, but it decomposes upon heating
Stability
Relatively stable in dry conditions, but sensitive to light, heat, and oxygen, which can lead to degradation
Absorption
Resveratrol is poorly absorbed in the human body, with only a small percentage being bioavailable
Metabolism
Rapidly metabolized in the liver and excreted in urine
Research
Ongoing studies are being conducted to better understand the potential health benefits, optimal dosages, and long-term effects of resveratrol supplementation.
Check Digit Verification of cas no
The CAS Registry Mumber 143207-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,0 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 143207-58:
(8*1)+(7*4)+(6*3)+(5*2)+(4*0)+(3*7)+(2*5)+(1*8)=103
103 % 10 = 3
So 143207-58-3 is a valid CAS Registry Number.
143207-58-3Relevant academic research and scientific papers
Synthesis and nematocidal activity of hydroxystilbenes
Ali,Kondo,Tsuda
, p. 1130 - 1136 (2007/10/02)
Various (E)-hydroxystilbenes were synthesized from (E)/(Z) mixtures of methoxystilbenes through a new (Z)-(E) isomerization method followed by demethylation. The nematocidal activity appears when methoxystilbenes are demethylated to hydroxystilbenes. For this activity, a hydroxy group at the C-2 or C-3 position is necessary. Thus, 2-hydroxy-, 3-hydroxy-, 2,6-dihydroxy-, 3,4-dihydroxy-, 3,5-dihydroxy-, 2,2'-dihydroxy-, 3,3'-dihydroxy-, 3,4'dihydroxy-, 2-hydroxy-4-methoxy-, 5-hydroxy-2-methoxy-, 2-hydroxy-6-methoxy-, 6-allyloxy-2-hydroxy-, 3-hydroxy-5-methoxy-, and 5-allyloxy-3-hydroxystilbenes showed rather potent nematocidal activity. The activity of 5-allyloxy-3-hydroxystilbene was the strongest [minimal lethal concentration (MLC) = 30 μM]. The activities of the (E) and (Z) isomers were comparable. The activities were also retained, though they were weaker, in the dihydro derivatives, hydroxybibenzyls.
