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34185-34-7

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34185-34-7 Usage

Molecular structure

2-(3-Hydroxyquinolin-2-yl)-cyclopentabnaphthalene-1,3-dione consists of a 3-hydroxyquinoline group attached to a cyclopenta[b]naphthalene-1,3-dione backbone.

Parent compound

It is a derivative of quinoline, which is an aromatic and heterocyclic compound.

Functional groups

The presence of the hydroxy group in the quinoline moiety can impart specific chemical reactivity and potential biological activity to the compound.

Potential applications

This compound may have potential applications in medicinal chemistry, organic synthesis, and materials science due to its unique combination of functional groups and aromatic moieties.

Further research

Further research and exploration of this compound may reveal its potential uses and properties in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 34185-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,8 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34185-34:
(7*3)+(6*4)+(5*1)+(4*8)+(3*5)+(2*3)+(1*4)=107
107 % 10 = 7
So 34185-34-7 is a valid CAS Registry Number.

34185-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-Hydroxy-2-quinolinyl)-1H-cyclopenta[b]naphthalene-1,3(2H)-di one

1.2 Other means of identification

Product number -
Other names Benzo-3'-hydroxychinophthalon

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:34185-34-7 SDS

34185-34-7Downstream Products

34185-34-7Relevant articles and documents

Isolation and identification of xenobiotic aryl hydrocarbon receptor ligands in dyeing wastewater

Chou, Pei-Hsin,Matsui, Saburo,Misaki, Kentaro,Matsuda, Tomonari

, p. 652 - 657 (2007)

Dyeing wastewater collected in Kyoto city, Japan, was investigated for the occurrence of aryl hydrocarbon receptor (AhR) ligands by using an AhR-responsive reporter gene assay. Concentrated extracts of wastewater samples elicited a dose-dependent increase in AhR ligand activity, and several hydrophobic HPLC fractions of the extracts were highly effective in inducing AhR ligand activity. Three potential AhR ligands were isolated from these fractions and identified to be Disperse Red 92, Disperse Yellow 64, and 3′-hydroxybenzo[b] quinophthalone by using HPLC and LC-MS/MS. Disperse Red 92, which has also been detected in the treated effluent from a sewage plant receiving the wastewater, is an anthraquinone disperse dye showing weak AhR binding affinity in the assay. Disperse Yellow 64 and 3′-hydroxybenzo[b]quinophthalone are quinoline disperse dyes capable of activating the AhR at nanomolar concentrations. In particular, Disperse Yellow 64 is a highly potent AhR ligand that was 3 times more effective in inducing AhR ligand activity than β-naphthoflavone in the assay. Quinoline disperse dyes are suggested to be a new class of xenobiotic AhR ligands which pose a danger to aquatic biota and human health.

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