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480-34-2

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480-34-2 Usage

Uses

Eugenin can be used for new phytoconstituents, anti-?microbial and cytotoxic activities.

Definition

ChEBI: A member of the class of chromones that is chromone substituted by a hydroxy group at position 5, a methoxy group at position 7 and a methyl group at position 2. It has been isolated from Pisonia aculeata.

Check Digit Verification of cas no

The CAS Registry Mumber 480-34-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 480-34:
(5*4)+(4*8)+(3*0)+(2*3)+(1*4)=62
62 % 10 = 2
So 480-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O4/c1-6-3-8(12)11-9(13)4-7(14-2)5-10(11)15-6/h3-5,13H,1-2H3

480-34-2SDS

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 eugenin

1.2 Other means of identification

Product number -
Other names 5-hydroxy-7-methoxy-2-methylchromen-4-one

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:480-34-2 SDS

480-34-2Relevant articles and documents

THREE CHROMONES FROM BULBS OF PANCRATIUM BIFLORUM

Ghosal, Shibnath,Singh, Shripati,Bhagat, Mahendra P.,Kumar, Yatendra

, p. 2943 - 2946 (1982)

Two polyoxygenated chromones, 5,7-dihydroxy-2-methylchromone (1) and 5,6-dihydroxy-7-methoxy-2-methylchromone (2), and a glucosyloxychromone, 7-glucosyloxy-5-hydroxy-2-methylchromone (3), have been isolated from an extract of the bulbs of Pancratium biflorum collected when the plants were in flower.The compounds were characterized by chemical transformation, comprehensive spectral evidence and synthesis. 2 and 3 are naturally occurring chromones, while 1 has been detected only once before in Daucus carota roots, as a stress metabolite. - Key Word Index: Panacratium biflorum; Amaryllidaceae; bulb; polyoxygenated chromones; 5,7-dihydroxy-2-methylchromone; 5,6-dihydroxy-7-methoxy-2-methylchromone; glucosyloxychromone; 7-glucosyloxy-5-hydroxy-2-methylchromone; chromone-metal complex.

Cytotoxic and HIF-1α inhibitory compounds from Crossosoma bigelovii

Klausmeyer, Paul,Zhou, Qin,Scudiero, Dominic A.,Uranchimeg, Badarch,Melillo, Giovanni,Cardellina, John H.,Shoemaker, Robert H.,Chang, Ching-Jer,McCloud, Thomas G.

body text, p. 805 - 812 (2009/12/26)

Cytotoxicity-guided fractionation of an organic solvent extract of the plant Crossosoma bigelovii led to the discovery of a new strophanthidin glycoside (1) and tw new 2-methylchromone glycosides (2 and 3). Also isolated were the known chromones eugenin a

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