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2-Hydroxylanosta-1,8,24-trien-3-one is a naturally occurring steroidal compound, specifically a triterpenoid, which is derived from the plant species Lanostane. This chemical is characterized by its unique molecular structure, featuring a hydroxyl group at the 2nd carbon position, and a carbonyl group at the 3rd position. It is known for its potential biological activities, such as anti-inflammatory and immunosuppressive properties, which are being studied for their potential applications in medicine. The compound's structure, with three double bonds at the 1st, 8th, and 24th carbon positions, contributes to its specific chemical reactivity and pharmacological effects. Research into 2-hydroxylanosta-1,8,24-trien-3-one and related compounds is ongoing to better understand their mechanisms of action and therapeutic potential.

20227-36-5

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20227-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20227-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,2 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20227-36:
(7*2)+(6*0)+(5*2)+(4*2)+(3*7)+(2*3)+(1*6)=65
65 % 10 = 5
So 20227-36-5 is a valid CAS Registry Number.

20227-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name LANOSTATRIEN-3-ONE-2-HYDROXY-

1.2 Other means of identification

Product number -
Other names 2-Hydroxylaminopyrene

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:20227-36-5 SDS

20227-36-5Downstream Products

20227-36-5Relevant academic research and scientific papers

SWERN OXIDATION OF α-KETOLS TO α-DIKETONES

Kawada, Kenji,Gross, Raymond S.,Watt, David S.

, p. 777 - 786 (2007/10/02)

The Swern oxidation of acyclic and cyclic α-ketols delivered α-diketones or the tautomeric diosphenols in good yield.

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