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Cyclolaudenone is a naturally occurring sesquiterpene lactone, a type of organic compound derived from plants, specifically found in the Artemisia annua plant, which is known for its antimalarial properties. It is characterized by a unique cyclic structure and exhibits various biological activities, including anti-inflammatory, anticancer, and antimicrobial effects. Cyclolaudenone has been studied for its potential therapeutic applications, particularly in the treatment of cancer and inflammatory diseases, due to its ability to modulate cellular processes and target specific enzymes.

2315-13-1

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2315-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2315-13-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,1 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2315-13:
(6*2)+(5*3)+(4*1)+(3*5)+(2*1)+(1*3)=51
51 % 10 = 1
So 2315-13-1 is a valid CAS Registry Number.

2315-13-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclolaudenone

1.2 Other means of identification

Product number -
Other names 9β,19-Cyclo-eburic-25-en-3-on

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:2315-13-1 SDS

2315-13-1Relevant academic research and scientific papers

Determination of the Absolute Configuration of Chiral Secondary Alcohols from Tetra-O-acetylglucosidation-Induced 1H Nuclear Magnetic Resonance Shifts

Faghih, Ramine,Fontaine, Catherine,Horibe, Isao,Immamura, Paulo M.,Lukacs, Gabor,et al.

, p. 4918 - 4920 (1985)

Tetra-O-acetylglucosidation-induced 1H nuclear magnetic resonance shifts were found highly characteristic of the absolute configuration of representative examples of R and S chiral secondary alcohols.The most important chemical shift changes of structurally diagnostic value for the determination of the absolute configuration of alcohols concern the protons of the aglycone attached to the carbons at β-position relative to the oxygen atom.

3-EPI-CYCLOLAUDENOL AND KNOWN TRITERPENES FROM EUPHORBIA CAUDICIFOLIA

Govardhan, Ch.,Prasad Reddy, R.,Sundararamaiah, T.

, p. 411 - 414 (2007/10/02)

A new tetracyclic triterpene, 3-epi-cyclolaudenol (24-methyl-9,19-cyclolanost-25-en-3α-ol), cyclolaudenol and cycloartenol were isolated from the ethanolic extract of the latex of Euphorbia caudicifolia, and cycloartenol and 3-ketomethylursolate were obtained from the ethanolic extract of the stem of this plant. - Keywords: Euphorbia caudicifolia; Euphorbiaceae; latex; stem; tetracyclic triterpenes; pentacyclic triterpenes; 3-epi-cyclolaudenol; cyclolaudenol; cycloartenol; 3-ketomethylursolate.

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