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Ethanone, 2-(4-nitrophenyl)-1-(2,4,6-trihydroxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15485-67-3

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15485-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15485-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,8 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15485-67:
(7*1)+(6*5)+(5*4)+(4*8)+(3*5)+(2*6)+(1*7)=123
123 % 10 = 3
So 15485-67-3 is a valid CAS Registry Number.

15485-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-nitrophenyl)-1-(2,4,6-trihydroxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 4-Nitrobenzyl 2,4,6-trihydroxyphenyl ketone

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:15485-67-3 SDS

15485-67-3Relevant academic research and scientific papers

Synthesis, Characterization, and Antioxidant Activities of Genistein, Biochanin A, and Their Analogues

Hamza Sherif, Salah,Gebreyohannes, BerihuTekluu

, (2018)

A series of naturally occurring genistein (3) and biochanin A (4) compounds and their analogues were synthesized from phloroglucinol. The structures of all the synthesized compounds were established by the combined use of 1HNMR, 13CNMR, IR spectral data, and mass spectrometry; their antioxidant activities were investigated. Most of the synthesized compounds show moderate-to-high activity; only two compounds exhibit no significant activity.

In vitro study of isoflavones and isoflavans as potent inhibitors of human 12- and 15-lipoxygenases

Mascayano, Carolina,Espinosa, Victoria,Sepulveda-Boza, Silvia,Hoobler, Eric K.,Perry, Steve

, p. 317 - 325 (2013/09/12)

In this study, we have investigated 16 isoflavone and isoflavan derivatives as potential inhibitors of human lipoxygenase (platelet 12-lipoxygenase, reticulocyte 15-lipoxygenase-1, and epithelial 15-lipoxygenase-2). The flavonoid baicalein, a known lipoxygenase inhibitor, was used as positive control. Four compounds, 6,7-dihydroxy-3′-chloroisoflavone (1c), 7-hydroxy-8-methyl-4′-chloroisoflavan (5a), 7,8-dihydroxy-4′-methylisoflavan (5b), and 7,8-dihydroxy-3′-methylisoflavan (5c), were effective inhibitors of 12-lipoxygenases and 15-lipoxygenase-1 with IC50's i values in the range of 0.3-3 μm.

Identification of isoflavone derivatives as effective anticryptosporidial agents in vitro and in vivo

Stachulski, Andrew V.,Berry, Neil G.,Low, Lilian A.C.,Moores, Shelley L.,Row, Eleanor,Warhurst, David C.,Adagu, Ipemida S.,Rossignol, Jean-Fran?ois

, p. 1450 - 1454 (2007/10/03)

We report the preparation and antiparasitic activity in vitro and in vivo of a series of isoflavone derivatives related to genistein. These analogues retain the 5,7-dihydroxyisoflavone core of genistein: direct genistein analogues (2-H isoflavones), 2-car

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