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(3beta)-lanostan-3-yl acetate is a chemical compound that belongs to the class of lanostanes, which are triterpenoids found in plants and fungi. It is derived from lanosterol, a precursor to cholesterol biosynthesis in humans, and has been identified in various natural sources such as the wood-rotting fungus Ganoderma lucidum. (3beta)-lanostan-3-yl acetate exhibits potential pharmacological properties such as anti-inflammatory, anti-tumor, and immunomodulatory activities, making it an important target for drug development and medicinal research. Its unique chemical structure and biological properties have attracted interest in potential therapeutic applications and further investigation into its mechanisms of action.

6562-14-7

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6562-14-7 Usage

Uses

Used in Pharmaceutical Industry:
(3beta)-lanostan-3-yl acetate is used as a pharmaceutical agent for its potential anti-inflammatory, anti-tumor, and immunomodulatory properties. Its ability to modulate various biological processes makes it a promising candidate for the development of new drugs to treat a range of diseases, including cancer and inflammatory conditions.
Used in Medicinal Research:
(3beta)-lanostan-3-yl acetate is used as a subject of medicinal research to further investigate its pharmacological properties and mechanisms of action. This research aims to better understand the compound's potential therapeutic applications and to develop new strategies for drug discovery and treatment.
Used in Drug Development:
(3beta)-lanostan-3-yl acetate is used in drug development as a starting point for the creation of new pharmaceuticals. Its unique chemical structure and biological properties provide a foundation for the design and synthesis of novel compounds with improved therapeutic efficacy and reduced side effects.
Used in Natural Product Chemistry:
(3beta)-lanostan-3-yl acetate is used in natural product chemistry to study the chemical constituents of plants and fungi, as well as their potential biological activities. This research contributes to the discovery of new bioactive compounds and the development of natural product-based drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 6562-14-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,6 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6562-14:
(6*6)+(5*5)+(4*6)+(3*2)+(2*1)+(1*4)=97
97 % 10 = 7
So 6562-14-7 is a valid CAS Registry Number.

6562-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [4,4,10,13,14-pentamethyl-17-(6-methylheptan-2-yl)-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate

1.2 Other means of identification

Product number -
Other names Essigsaeure-indan-5-ylester

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:6562-14-7 SDS

6562-14-7Relevant academic research and scientific papers

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