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(3aS,4R,9aS)-4-(3,4-dihydroxyphenyl)-6,7-dihydroxy-3a,4,9,9a-tetrahydronaphtho[2,3-c]furan-1(3H)-one is a complex organic compound featuring a naphthofuran scaffold, a phenyl ring, and multiple hydroxyl groups. Its unique molecular structure endows it with potential antioxidant and anti-inflammatory properties, positioning it as a promising candidate for pharmaceutical applications, particularly in the development of drugs targeting cancer and neurodegenerative diseases.

2316-10-1

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2316-10-1 Usage

Uses

Used in Pharmaceutical Industry:
(3aS,4R,9aS)-4-(3,4-dihydroxyphenyl)-6,7-dihydroxy-3a,4,9,9a-tetrahydronaphtho[2,3-c]furan-1(3H)-one is used as a potential therapeutic agent for the development of drugs targeting cancer and neurodegenerative diseases due to its antioxidant and anti-inflammatory properties. Further research is required to fully understand its biological activity and therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 2316-10-1 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 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2316-10:
(6*2)+(5*3)+(4*1)+(3*6)+(2*1)+(1*0)=51
51 % 10 = 1
So 2316-10-1 is a valid CAS Registry Number.

2316-10-1SDS

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 (3aS,4R,9aS)-4-(3,4-dihydroxyphenyl)-6,7-dihydroxy-3a,4,9,9a-tetrahydro-3H-benzo[f][2]benzofuran-1-one

1.2 Other means of identification

Product number -
Other names CONIDENDROL,DIHYDRATE

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:2316-10-1 SDS

2316-10-1Upstream product

2316-10-1Relevant academic research and scientific papers

A selective de-O-methylation of guaiacyl lignans to corresponding catechol derivatives by 2-iodoxybenzoic acid (IBX). the role of the catechol moiety on the toxicity of lignans

Bernini, Roberta,Barontini, Maurizio,Mosesso, Pasquale,Pepe, Gaetano,Willfoer, Stefan M.,Sjoeholm, Rainer E.,Eklund, Patrik C.,Saladino, Raffaele

experimental part, p. 2367 - 2377 (2009/09/26)

We report here the first selective de-O-methylation of a large panel of guaiacyl lignans to the corresponding catechol derivatives by using IBX as primary oxidant under green conditions (dimethyl carbonate-H2O solvent) through an in situ reduction procedure. The influence of the catechol moiety on the cytotoxicity and genotoxicity of new lignan derivatives has been investigated. The results obtained indicated that the presence of the catechol moiety sharply enhances the clastogenic potential (e.g. induction of chromosomal aberrations), the cytotoxicity and the modulation of cell cycle progression with respect to the parent compounds. Thus, despite the in vitro antioxidant activity usually described for catechol derivatives, our results show for the first time the generation of a clastogenic potential, highly indicative of a long-term genetic and cancer risk. The Royal Society of Chemistry 2009.

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