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The chemical compound "6-hydroxy-6,10,14-trimethyl-3-methylidene-3a,4,5,6,7,8,11,12,13,14,15,15a-dodecahydro-5,15-epoxycyclotetradeca[b]furan-2(3H)-one" is a complex organic molecule with a unique structure. It features a cyclotetradeca[b]furan ring system, which is a type of cyclic compound with a furan ring fused to a cyclotetradecane ring. The molecule contains three methyl groups at positions 6, 10, and 14, and a methylidene group at position 3, which contributes to its stability and reactivity. Additionally, it has a hydroxyl group at position 6, indicating the presence of an alcohol functional group. The compound also includes a dodecahedral hydrocarbon framework, with 12 carbon atoms forming a three-dimensional structure. The 5,15-epoxy bridge further adds to the complexity of the molecule, making it a potentially interesting candidate for various chemical and pharmaceutical applications due to its intricate structure and functional groups.

55822-19-0

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55822-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55822-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,2 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55822-19:
(7*5)+(6*5)+(5*8)+(4*2)+(3*2)+(2*1)+(1*9)=130
130 % 10 = 0
So 55822-19-0 is a valid CAS Registry Number.

55822-19-0SDS

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 Eunicin

1.2 Other means of identification

Product number -
Other names CUEUNICIN

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:55822-19-0 SDS

55822-19-0Upstream product

55822-19-0Downstream Products

55822-19-0Relevant academic research and scientific papers

Synthesis of cytotoxic cembranolide analogues via acid-induced opening of oxiranes

Rodríguez, Abimael D.,Pi?a, Ivette C.,Acosta, Ana L.,Barnes, Charles L.

, p. 93 - 107 (2001)

A large series of analogues of Eunicea cembranolides 1-3 were synthesized with the purpose of evaluating their cytotoxicity against 60 human cancer cell-lines. Most of the analogues were as active as the lead compounds and a few displayed increased cytotoxicity. Their syntheses were based on the specific reactivity and stereochemistry of the epoxide substructure and involved highly regio- and diastereoselective acid-induced chemical transformations.

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