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471-67-0

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471-67-0 Usage

Triterpene compound

18BETA(H)-OLEANANE is a compound derived from plants, specifically from the triterpenoid group.

Ursane type

It belongs to the ursane type of triterpenoids, which is a subgroup of triterpenes.

Molecular structure

The compound has a unique molecular structure that includes a pentacyclic ring system.

Biological activities

18BETA(H)-OLEANANE has been found to possess various biological activities, such as anti-inflammatory, anti-tumor, and antiviral properties.

Wound healing

The compound has shown potential in promoting wound healing.

Oxidative stress protection

18BETA(H)-OLEANANE has been found to protect against oxidative stress.

Therapeutic potential

Studies have suggested that 18BETA(H)-OLEANANE may have a therapeutic potential in treating a range of diseases, making it an interesting target for further research and potential pharmaceutical development.

Check Digit Verification of cas no

The CAS Registry Mumber 471-67-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 471-67:
(5*4)+(4*7)+(3*1)+(2*6)+(1*7)=70
70 % 10 = 0
So 471-67-0 is a valid CAS Registry Number.

471-67-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicene

1.2 Other means of identification

Product number -
Other names oleanane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:471-67-0 SDS

471-67-0Downstream Products

471-67-0Relevant articles and documents

-

Ruzicka et al.

, (1938)

-

Reduction of Steroid and Triterpenoid α,β-Unsaturated Ketones with Lithium/Ethylenediamine

Pradhan, Bhim Prasad,Chakraborty, Satyajit

, p. 263 - 265 (2007/10/02)

Reduction of less sterically hindered ketone, glochidone (1) with lithium/ethylenediamine (Li/EDA) leads to the reduction of the double bond followed by that of the carbonyl group to afford thermodynamically stable alcohol, lupanol (1b).The sterically hindered α,β-unsaturated ketones such as 11-keto-triterpenoids also furnish saturated alcohols but in small proportions; the other compounds formed are obtained with reduction of the carbonyl group accompanied by dehydration or even deoxygenation.

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