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Alepterolic acid is a bioactive chemical compound, a derivative of betulinic acid, that is commonly found in various species of wild plants. It exhibits several therapeutic and pharmaceutical properties, with studies suggesting its potential in anti-inflammatory, antimalarial, and anticancer activities. Alepterolic acid is known for its cytotoxic characteristics against human cancer cells, although more comprehensive research is needed to fully understand its bioactive properties and possible side effects in medical applications.

63399-38-2

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63399-38-2 Usage

Uses

Used in Pharmaceutical Industry:
Alepterolic acid is used as a therapeutic agent for its potential anti-inflammatory properties, which may help in reducing inflammation and related symptoms in various conditions.
Used in Antimalarial Applications:
Alepterolic acid is used as an antimalarial agent, potentially providing a treatment option for combating malaria, a disease caused by parasites that infect red blood cells.
Used in Anticancer Applications:
Alepterolic acid is used as an anticancer agent, particularly for its cytotoxic effects on human cancer cells. It may play a role in inhibiting tumor growth and progression, although further research is required to confirm its efficacy and safety in this context.
Used in Drug Development Research:
Alepterolic acid is used as a subject of study in drug development research, as its bioactive properties and potential side effects are further investigated to determine its suitability for various medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 63399-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,9 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63399-38:
(7*6)+(6*3)+(5*3)+(4*9)+(3*9)+(2*3)+(1*8)=152
152 % 10 = 2
So 63399-38-2 is a valid CAS Registry Number.

63399-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-5-[(1S,4aR,6S,8aR)-6-Hydroxy-5,5,8a-trimethyl-2-methylenedec ahydro-1-naphthalenyl]-3-methyl-2-pentenoic acid

1.2 Other means of identification

Product number -
Other names 3-Penten-2-one,3-methyl-4-phenyl

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:63399-38-2 SDS

63399-38-2Downstream Products

63399-38-2Relevant academic research and scientific papers

Synthesis of (+/-)-karahana ether and a (+/-)-labdadienoic acid by the electrophilic cyclization of epoxy allylsilanes

Armstrong, Rosemary J.,Weiler, Larry

, p. 584 - 596 (2007/10/02)

The epoxy allylsilanes 7 and 16 were synthesized by stereoselective routes from β-keto esters and cyclized with Lewis acids in good yield.The monocyclic product from 7 was converted into (+/-)-karahana ether (10), and the bicyclic product from 20 was used in a synthesis of the 3-hydroxylabdadienoic acid 24b.

DERIVATIVES OF ANTICOPALIC ACID AND OTHER NEW COMPOUNDS FROM THE OLEORESIN OF Pinus pumila

Raldugin, V. A.,Pentegova, V. A.

, p. 149 - 154 (2007/10/02)

From the oleoresin of the Japanese stone pine the previously known agatholic, agathalic, agathic and 3β-hydroxyanticopalic acids, and also the new acids 19-methoxyanticopalic and 19-O-succinylagatholic acids have been isolated and identified in the form of their methyl esters.Two new esters of 1-borneol have been isolated and characterized in the form of their acetates - the ferulate and the p-coumarate.

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