5356-56-9

Basic information

• Product Name: β-AMyrenonol acetate
• Synonyms: β-AMyrenonol acetate;beta-Amyrenonol acetate
• CAS NO: 5356-56-9
• Molecular Formula: C7H10O4
• Molecular Weight: 158.1519
• Mol File: 5356-56-9.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 339.8°Cat760mmHg
• Flash Point: 159.3°C
• Appearance: /
• Density: 1.556g/cm³
• Vapor Pressure: 8.98E-05mmHg at 25°C
• Refractive Index: 1.706
• CAS DataBase Reference: β-AMyrenonol acetate(CAS DataBase Reference)
• NIST Chemistry Reference: β-AMyrenonol acetate(5356-56-9)
• EPA Substance Registry System: β-AMyrenonol acetate(5356-56-9)

Safety Data

• Hazardous Substances Data: 5356-56-9(Hazardous Substances Data)

Usage

Description

β-Amyrenonol acetate is a triterpenoid, a type of organic compound derived from natural plant sources such as tobacco. It possesses unique chemical properties and has been studied for its potential medicinal properties, including anti-inflammatory and antibacterial effects. Its structure makes it a valuable compound for various industrial and medicinal applications.

Uses

Used in Pharmaceutical Industry:
β-Amyrenonol acetate is used as a potential medicinal compound for its anti-inflammatory and antibacterial effects. It is being investigated for its potential use in the development of new pharmaceuticals to treat various conditions.
Used in Commercial Applications:
β-Amyrenonol acetate is used in a variety of commercial applications due to its unique chemical structure and properties. Its versatility makes it a valuable compound for different industries.

InChI:InChI=1/C11H7ClN2O3S/c12-7-3-4-8(9(6-7)14(16)17)13-11(15)10-2-1-5-18-10/h1-6H,(H,13,15)

Upstream product

• 38242-02-3 11-oxo-β-amyrin 
• 108-24-7 acetic anhydride 
• 7446-08-4 selenium(IV) oxide 
• 2118-76-5 olean-9(11),12(13)-dien-3β-yl acetate 
• 7732-18-5 water 
• 127-09-3 sodium acetate 
• 64-19-7 acetic acid 
• 1616-93-9 β-Amyrin-acetat 
• 2118-84-5 3β-benzoyloxy-oleanen-(12)-one-(11) 
• 1616-93-9 β-amyrin acetate 
• 559-70-6 β-amyrin 
• 1616-93-9 β-amyrin acetate 

Downstream Products

• 38242-02-3 11-oxo-β-amyrin 
• 38242-02-3 3β-hydroxy-18α-oleanen-(12)-one-(11) 
• 94530-87-7 3β-hydroxy-olean-9(11),12-diene 
• 471-67-0 oleanane 
• 113504-43-1 oleanan-3β,11α-diol 
• 2118-75-4 3β-acetoxy-oleana-11,13(18)-diene 
• 2118-76-5 olean-9(11),12(13)-dien-3β-yl acetate 
• 5356-55-8 11α-hydroxy-3β-acetoxy-olean-12-ene 
• 94530-87-7 oleana-9(11),12-dien-3-β-ol 

Relevant articles and documents

New peroxy triterpenes from the aerial roots of Ficus microcarpa

Six new triterpenes, 3β-acetoxy-12β, 13β-epoxy-11α-hydroperoxyursane (1), 3β-acetoxy-11α-hydroperoxy-13αH-ursan-12-one (2), 3β-acetoxy-1β, 11α-epidioxy-12-ursene (3), (20S)-3β-acetoxylupan-29-oic acid (4), (20S)-3β-acetoxy-20-hydroperoxy-30-norlupane (5),

Oxidation of Terpenoid Compounds with tert-Butyl Chromate

Oxidation with tert-butyl chromate of a methylene group adjacent to a double bond or aromatic ring has been effected in excellent yield with the majority of a selected group of diterpenes and triterpenes.Some of the factors influencing the course of the reaction are discussed.Keywords - oxidation; tert-butyl chromate; diterpene; triterpene; ketone

Phase-transfer Catalysed Allylic Oxidation of Hindered Double Bonds in a Rigid Framework by Sodium Periodate

The reaction of sodium periodate under phase-transfer catalysis with abietenol acetate-diethyl fumarate Diels-Alder adduct (1), β-amyrin acetate (3) and α-amyrin acetate (4) furnishes allylic oxygenated products 2, 5 and 6 respectively.This appears to be the first report of allylic oxidation by sodium periodate.