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96284-36-5

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96284-36-5 Usage

Description

(3beta,5xi,18alpha)-3,24-dihydroxyolean-12-ene-28,29-dioic acid is a triterpenoid compound, a class of organic compounds that can be found in various plants, especially in herbs used in traditional medicine. It has been studied for its potential pharmacological properties, such as anti-inflammatory and antioxidant effects, and has shown promising results in preclinical studies as a potential therapeutic agent for various diseases, including cancer and diabetes.

Uses

Used in Pharmaceutical Industry:
(3beta,5xi,18alpha)-3,24-dihydroxyolean-12-ene-28,29-dioic acid is used as a potential therapeutic agent for various diseases, such as cancer and diabetes, due to its pharmacological properties, including anti-inflammatory and antioxidant effects.
Used in Research and Development:
(3beta,5xi,18alpha)-3,24-dihydroxyolean-12-ene-28,29-dioic acid is used as a subject of interest for further research in the fields of pharmacology and natural product chemistry, due to its complex structure and biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 96284-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,8 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96284-36:
(7*9)+(6*6)+(5*2)+(4*8)+(3*4)+(2*3)+(1*6)=165
165 % 10 = 5
So 96284-36-5 is a valid CAS Registry Number.

96284-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,4aR,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-10-hydroxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2,4a-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:96284-36-5 SDS

96284-36-5Upstream product

96284-36-5Downstream Products

96284-36-5Relevant articles and documents

New approaches to the structural modification of olean-type pentacylic triterpenes via microbial oxidation and glycosylation

Zhu, Yu-Yao,Qian, Li-Wu,Zhang, Jian,Liu, Ji-Hua,Yu, Bo-Yang

, p. 4206 - 4211 (2011)

Microbial transformation of 4 olean-type pentacyclic triterpenes (OPTs), 3-oxo oleanolic acid (1), 3-acetyl oleanolic acid (2), oleanolic acid (3), and esculentoside A (4) was studied. After the screening of 12 strains of microbes, preparative biotransformation by two strains of Streptomyces griseus ATCC 13273 and Aspergillus ochraceus CICC 40330 resulted in the isolation of 10 metabolites. The microbial catalyzed high efficient regio-selective methyl oxidation and glycosylation were discovered, which could be provided as an alternative method to expand the structural diversity of OPTs. All the structures of the metabolites were elucidated unambiguously by ESI-MS, 1H NMR, 13C NMR, and 2D-NMR spectroscopy.

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