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1-Naphthalenecarboxaldehyde, 2-hydroxy-, (phenylmethylene)hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56024-39-6

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56024-39-6 Usage

Properties

It is a hydrazone derivative.
Has potential as an antifungal and anti-inflammatory agent.
Has potential as a corrosion inhibitor for metals.
May be useful for research in organic chemistry and materials science.
Potential for industrial applications in pharmaceuticals or materials coatings.

Specific content

1-Naphthalenecarboxaldehyde, 2-hydroxy-, (phenylmethylene)hydrazone is a chemical compound.
It has a specific structure and properties that make it potentially useful in various applications.
Further study and research is needed to fully understand and utilize its potential.

Check Digit Verification of cas no

The CAS Registry Mumber 56024-39-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,2 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56024-39:
(7*5)+(6*6)+(5*0)+(4*2)+(3*4)+(2*3)+(1*9)=106
106 % 10 = 6
So 56024-39-6 is a valid CAS Registry Number.

56024-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxynaphthalin-1-carbaldehyd-benzyliden-hydrazon

1.2 Other means of identification

Product number -
Other names 1-{[1-Phenyl-meth-(E)-ylidene]-hydrazonomethyl}-naphthalen-2-ol

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:56024-39-6 SDS

56024-39-6Downstream Products

56024-39-6Relevant academic research and scientific papers

Dual mode ratiometric recognition of zinc acetate: Nanomolar detection with in vitro tracking of endophytic bacteria in rice root tissue

Ghosh, Abhijit,Ta, Sabyasachi,Ghosh, Milan,Karmakar, Subhajit,Banik, Avishek,Dangar, Tushar Kanti,Mukhopadhyay, Subhra Kanti,Das, Debasis

, p. 599 - 606 (2015)

Several naphthalene-based aldazine derivatives were developed as efficient colorimetric and fluorescence probes for selective ratiometric recognition of traces of zinc acetate. The derivative structures were characterized by single-crystal X-ray diffraction. The probes were used for in vitro tracking of zinc acetate in endophytic bacteria within rice root tissue and to image zinc acetate in human breast cancer cells (MCF7) by normal and fluorescence microscopy. Density functional theoretical studies were in close agreement with the experimental findings.

White-light emission from simple AIE-ESIPT-excimer tripled single molecular system

Samanta, Soham,Manna, Utsab,Das, Gopal

, p. 1064 - 1072 (2017)

A simple organic molecule (L3) has been systematically designed and developed to generate white-light emission from a single-component system. It could also tune several emission colors owing to its diverse spectral nature with varying water fractions in methanol-water and acetonitrile-water mixtures. Essentially, the introduction of an aggregation-induced emission (AIE) phenomenon and excimer-forming ability in the molecular system provided the scope for a dual emission, whereas ESIPT (excited state intramolecular proton transfer) coupled-AIE phenomenon acted as an additional means of adjusting the emission wavelength of the corresponding emission peak by varying the solvent polarity. Detailed AFM (atomic force microscopy), DLS (dynamic light scattering) and X-ray crystallographic studies were carried out to validate the mechanism of generation of white-light emission.

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