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(3alpha,5xi,18alpha)-olean-12-en-3-ol is a naturally occurring triterpenoid compound, characterized by its unique molecular structure with a 3-hydroxyl group at the 3alpha position, a double bond at the 5xi position, and a 12-en bond at the 18alpha position. This chemical is derived from the oleanane family of triterpenoids, which are known for their diverse range of biological activities, including anti-inflammatory, anti-cancer, and immunomodulatory effects. Found in various plant species, particularly in the Olea europaea (olive) tree, (3alpha,5xi,18alpha)-olean-12-en-3-ol has been the subject of scientific research due to its potential therapeutic applications. Its structure and properties make it a promising candidate for further study in the development of new drugs and natural remedies.

6811-63-8

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6811-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6811-63-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,1 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6811-63:
(6*6)+(5*8)+(4*1)+(3*1)+(2*6)+(1*3)=98
98 % 10 = 8
So 6811-63-8 is a valid CAS Registry Number.

6811-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names Olean-12-en-3-ol, (3α)-

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:6811-63-8 SDS

6811-63-8Relevant academic research and scientific papers

A short enantioselective total synthesis of the fundamental pentacyclic triterpene lupeol

Surendra, Karavadhi,Corey

supporting information; experimental part, p. 13928 - 13929 (2009/12/25)

(Chemical Equation Presented) The first enantioselective synthesis of lupeol has been developed by applying two carefully crafted cation-π cyclization stages to generate the pentacyclic structure with complete stereocontrol. The synthesis (Scheme 1) is no

An antidepressant principle of Lobelia inflata L. (Campanulaceae)

Subarnas,Oshima,Sidik,Ohizumi

, p. 620 - 621 (2007/10/02)

A crude methanolic extract of the leaves of Lobelia inflata exhibited antidepressant activity in mice. The extract was fractionated, monitored by the activity, to give β-amyrin palmitate as an active component.

REDUCTION OF KETONES TO EPIMERIC ALCOHOLS WITH POTASSIUM HYDROXIDE-DIETHYLENE GLYCOL

Pradhan, B. P.,Hassan, A.,Ray, T.

, p. 2513 - 2516 (2007/10/02)

Triterpenoid ketones have been reduced to epimeric alcohols on boiling with potassium hydroxide in diethylene glycol. α,β-unsaturated ketone furnished saturated epimeric alcohols.

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