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Anemonine is a toxic chemical compound found in certain plants of the Ranunculaceae family, such as anemone and buttercup. It is a lactone derivative of the unsaturated diterpene, protoanemonin, and is responsible for the plants' bitter taste and toxic properties. Despite its toxicity, anemonine has been studied for its potential biological activities, including antimicrobial, antifungal, and anti-inflammatory properties.

508-44-1

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508-44-1 Usage

Uses

Used in Pharmaceutical Industry:
Anemonine is used as a potential pharmaceutical candidate for its antimicrobial, antifungal, and anti-inflammatory properties. However, due to its high toxicity, it requires careful handling and formulation to minimize adverse effects on humans and animals.
Used in Research and Development:
Anemonine is used in research and development for studying its biological activities and potential applications in medicine. It can provide insights into the development of new drugs and therapies targeting various diseases and conditions.
Used in Plant Defense Mechanisms:
Anemonine plays a role in the defense mechanisms of plants containing it, as its toxic properties help protect the plants from being consumed by herbivores and other organisms.

Check Digit Verification of cas no

The CAS Registry Mumber 508-44-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 508-44:
(5*5)+(4*0)+(3*8)+(2*4)+(1*4)=61
61 % 10 = 1
So 508-44-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O4/c11-7-1-3-9(13-7)5-6-10(9)4-2-8(12)14-10/h1-4H,5-6H2/t9-,10-/m1/s1

508-44-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,7-Dioxadispiro[4.0.4.2]dodeca-3,9-diene-2,8-dione

1.2 Other means of identification

Product number -
Other names 1,7-Dioxadispiro[4.0.4.2]dodeca-3,9-diene-2,8-dione, trans-

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:508-44-1 SDS

508-44-1Relevant academic research and scientific papers

STUDIES ON STRUCTURALLY SIMPLE α,β-BUTENOLIDES-I NEW SYNTHESIS OF RACEMIC γ-HYDROXYMETHYL-α,β-BUTENOLIDE AND DERIVATIVES

Cardellach, J.,Estopa, C.,Font, J.,Moreno-Manas, M.,Ortuno, R. M.,et al.

, p. 2377 - 2394 (2007/10/02)

Exhaustive approaches to the synthesis of racemic γ-heterosubstituted γ-methyl-α,β-butenolides are presented, starting from C3 synthons (glyceraldehyde, glycidaldehyde, acrolein and 2,3-epoxypropyl ethers).Good general methods for the preparation of γ-hydroxymethyl-α,β-butenolide 2, several of its ether derivatives, as well as of γ-bromomethyl-α,β-butenolide 5, are given.The reactivities of these structurally simple but highly functionalized compounds, convenient synthons for more complex molecules, are preliminarily explored.

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