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117591-81-8

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    Cas No: 117591-81-8

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117591-81-8 Usage

General Description

Coronarin E is a chemical compound belonging to the class of flavonoids, which are naturally occurring compounds found in various plants, particularly in the Lamiaceae family. It has been identified in high levels in the leaves of the plant Teucrium polium L., a member of the Lamiaceae family, and has been studied for its potential medicinal properties. Coronarin E has been found to possess antioxidant, anti-inflammatory, and antiproliferative properties, making it a potential candidate for the development of new therapeutic agents for various conditions. Research on Coronarin E is ongoing and it shows promise for its potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 117591-81-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,5,9 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 117591-81:
(8*1)+(7*1)+(6*7)+(5*5)+(4*9)+(3*1)+(2*8)+(1*1)=138
138 % 10 = 8
So 117591-81-8 is a valid CAS Registry Number.

117591-81-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Coronarin E

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:117591-81-8 SDS

117591-81-8Relevant articles and documents

Lewis Acid-Catalyzed Stereoselective α-Addition of Chiral Aldehydes to Cyclic Dienol Silanes: Aqueous Synthesis of Chiral Butenolides

Adamkiewicz, Anna,W?glarz, Izabela,Butkiewicz, Aleksandra,Woyciechowska, Marta,Mlynarski, Jacek

, p. 667 - 678 (2019/12/24)

The stereoselective α-addition to cyclic dienol silanes has rarely been exploited, in contrast to the well-studied γ-addition of conjugated butenolides. In this study, an unprecedent catalytic Mukaiyama aldol α-addition of 2-trimetylsiloxy furan to optically pure aldehydes in water-containing solvents is reported. The synthetic utility of this concept was demonstrated in the efficient synthesis of six bioactive natural products: vitexolide D, curcucomosin C, villosin, chinensine C, (+)-coronarin E and (E)-labda-7,11,13-trien-16,15-olid.

Synthesis of chinensines A-E

Margaros, Ioannis,Vassilikogiannakis, Georgios

, p. 4826 - 4831 (2008/02/05)

(Chemical Equation Presented) Short and efficient syntheses of coronarin E (4) and chinensines A-E (5-9) have been accomplished. The use of two different types of reaction of singlet oxygen (1O2) lies at the heart of the synthetic st

Facile Access to Optically Active Labdane-Type Diterpenes from (+)-Manool. Synthesis of (+)-Coronarin E, (+)-15,16-Epoxy-8(17),13(16),14-labdatriene, and (+)-Labda-8(17),13(Z)-diene-15,16-diol

Villamizar, Jose,Fuentes, Juan,Salazar, Franklin,Tropper, Eleonora,Alonso, Randolph

, p. 1623 - 1627 (2007/10/03)

An efficient method for the synthesis of (+)-coronarin E (1), (+)-15,16-epoxy-8(17),13(16),14-labdatriene (2), and (+)-labda-8(17),13(Z)-diene-15,16-diol (3) from (+)-manool is described.

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