20460-33-7

Basic information

• Product Name: Epitaraxerol
• Synonyms: Epitaraxerol;Isotaraxerol
• CAS NO: 20460-33-7
• Molecular Formula: C₃₀H₅₀O
• Molecular Weight: 426.72
• Mol File: 20460-33-7.mol
• Article Data: 8

Chemical Properties

• Melting Point: 257-258 °C
• Boiling Point: 490.7±44.0 °C(Predicted)
• Appearance: /
• Density: 1.01±0.1 g/cm3(Predicted)
• PKA: 15.19±0.70(Predicted)
• CAS DataBase Reference: Epitaraxerol(CAS DataBase Reference)
• NIST Chemistry Reference: Epitaraxerol(20460-33-7)
• EPA Substance Registry System: Epitaraxerol(20460-33-7)

Safety Data

• Hazardous Substances Data: 20460-33-7(Hazardous Substances Data)

Usage

General Description

Epitaraxerol is a naturally occurring chemical compound found in the plant Tanacetum parthenium, commonly known as feverfew. It is a sesquiterpene lactone and has been found to have anti-inflammatory and anti-cancer properties. Epitaraxerol has been studied for its potential in inhibiting the growth of cancer cells and reducing inflammation in the body. It is also being researched for its potential in treating migraines, as feverfew has traditionally been used for this purpose. The compound is still being studied for its potential applications in medicine and pharmacology.

Upstream product

• 514-07-8 taraxerone 
• 123-51-3 i-Amyl alcohol 
• 514-07-8 Taraxerone 
• 2189-80-2 taraxeryl acetate 
• 141-78-6 ethyl acetate 

Downstream Products

• 514-07-8 taraxerone 
• 1679-02-3 2,9-dimethyl-picene 
• 2189-80-2 taraxeryl acetate 
• 1269649-38-8 taraxerol 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->3)-[2,3,4-tri-O-acetyl-α-L-rhamnopyransyl-(1->2)]-4,6-di-O-benzylidene-β-D-galactopyranoside 
• 2189-80-2 Taraxerol-acetat 
• 14021-23-9 taraxerol methyl ether 
• 79806-73-8 taraxerol-3β-tosylate 
• 10388-60-0 3β-benzoyloxy-D-friedo-olean-14-ene 
• 582-16-1 2,7-dimethylnaphthalene 
• 488-23-3 1,2,3,4-Tetramethylbenzene 
• 2131-43-3 1,2,5,6-tetramethylnaphthalene 
• 486-34-0 1,2,7-trimethylnaphthalene 

Relevant articles and documents

Triterpenes from the Leaves of Parsonsia Laevigata

A novel taraxerane-type triterpene-diol, in addition to taraxerol and lupeol, was isolated from the leaves of Parsonsia laevigata.Its structure was shown to be (4β)-D-friedoolean-14-ene-3β,24-diol (taraxer-14-ene-3β,24-diol) by a combination of chemical and spectroscopic methods.Key Word Index - Parsonsia laevigata; Apocynaceae; taraxerane-type triterpenoid; (4β)-D-friedoolean-14-ene-3β,24-diol.

Terpenoids and Related Compounds: Part XXXI - Stereospecific Reduction of Triterpenoid Ketones with Lithium and Ethylenediamine

Hindered triterpenoid ketones are reduced in excellent yields to the corresponding thermodynamically more stable alcohols on stereospecific reduction with lithium and ethylenediamine.

Triterpenoids of the Bark of Pieris japonica D. Don (Japenese Name: Asebi). II. 13C Nuclear Magnetic Resonance of the γ-Lactones of Ursane- and Oleane-type Triterpenes

Eight triterpenoids and a sterol were isolated from the bark of Pieris japonica D.Don (Japenese name: asebi, Ericaceae) and have been elucidated as 3β-acetoxyurs-11-en-28,13-olide, 3β-acetoxy-12α-hydroxyolean-28,13-olide, 3β-acetoxy-28-hydroxyurs-12-ene, 3β,28-dihydroxyurs-12-ene, 3β-acetoxyurs-12-en-28-al, taraxeryl-acetate, taraxerol, taraxerone and β-sitosterone by a combination of chemical and spectroscopic studies. 13C Nuclear magnetic resonance spectral analysis of several γ-lactones of the ursane and oleanane series was undertaken, and all the carbons were assigned by means of single frequency off-resonance and selective decoupling methods and by comparison of the signals with those of methyl esters of acetyl ursolic acid and acetyl oleanolic acid.Keywords - Pieris japonica; bark; triterpenoid; ursane-type γ-lactone; oleanane-type γ-lactone; 1H-NMR; 13C-NMR