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Ethanone, 1-[4-[(2-hydroxy-1-naphthalenyl)azo]phenyl]-, also known as 1-[4-[(2-hydroxy-1-naphthalenyl)azo]phenyl]ethanone, is a complex organic compound with the molecular formula C19H15N3O2. It is characterized by a unique structure that includes a naphthalene ring, an azo group, and a phenyl ring, all connected through various functional groups. This chemical is primarily used as a dye or pigment in various industrial applications, such as coloring textiles, plastics, and other materials. Due to its complex structure, it may exhibit specific chemical properties and reactivity patterns, making it a subject of interest in the field of organic chemistry and material science.

4928-58-9

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4928-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4928-58-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,2 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4928-58:
(6*4)+(5*9)+(4*2)+(3*8)+(2*5)+(1*8)=119
119 % 10 = 9
So 4928-58-9 is a valid CAS Registry Number.

4928-58-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(4-acetylphenyl)hydrazinylidene]naphthalen-2-one

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

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

More Details:4928-58-9 SDS

4928-58-9Downstream Products

4928-58-9Relevant academic research and scientific papers

Novel chromenes and benzochromenes bearing arylazo moiety: molecular docking, in-silico admet, in-vitro antimicrobial and anticancer screening

Afifi, Tarek H.,Riyadh, Sayed M.,Deawaly, Anwar A.,Naqvi, Arshi

, p. 1471 - 1487 (2019)

Novel derivatives of benzochromene 9a–e and chromene 10a–e were synthesized via multi components reaction that utilizes azo dyes, malononitrile, and arylaldehydes as starting materials. The structures of the newly synthesized compounds were elucidated by the IR, 1H-NMR, 13C-NMR and mass spectral data. The new synthesized compounds were explored for their in-silico ADMET properties. The docking investigations verified good docking outcomes in terms of score and binding affinities of the examined compounds on the desired proteins, namely the GlcN-6-P synthase and PI3Ks. The in-vitro studies, which encompassed the antibacterial activity against two types of Gm +ve and two of Gm –ve, and the antifungal activity against four fungi micro-organisms were evaluated by the well diffusion method for the synthesized compounds. Moreover, the anticancer activity was tested against three human carcinoma cell lines [human colon carcinoma (HCT-116), human breast adenocarcinoma (MCF-7), and liver carcinoma (HEPG-2)], exhibiting promising anticancer activity in comparison to Vinblastine, Colchicine and Doxorubicin as standard drugs. The data suggests that some of the new derivatives of chromene scaffold which emerged promising in the in-silico molecular docking studies displayed good in-vitro antimicrobial and anticancer activities and could be exploited as leads for further optimization.

Synthesis of new spin probes based on aminoaryl-substituted imidazoline nitroxides

Reznikov, V. A.,Berezina, T. A.,Kirilyuk, I. A.,Volodarskii, L. B.

, p. 424 - 427 (2007/10/02)

A series of new spin probes, azides and isothiocyanates, were synthesized starting from aminoaryl-substituted nitroxides which are derivatives of 3-imidazoline and 3-imidazoline-3-oxide.The new compounds were transformed to complexones, derivatives of iminodiacetic acid. - Key words: nitroxyl radical; azides; isothiocyanates; spin probes; diazonium salts.

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