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1-{[(4-hydroxyphenyl)amino]methylidene}naphthalen-2(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

894-96-2

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894-96-2 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This describes the specific arrangement of atoms and bonds in the compound, including the naphthalen-2(1H)-one core, the hydroxyphenylamine group, and the methylidene group.
3. Synthetic organic compound

Explanation

The compound is artificially synthesized and belongs to the class of organic compounds, which are primarily composed of carbon and hydrogen atoms.
4. Derivative of naphthalen-2(1H)-one

Explanation

The compound is derived from the parent compound naphthalen-2(1H)-one, which is a type of aromatic ketone.
5. Contains hydroxyphenylamine group

Explanation

The compound has a hydroxyphenylamine functional group, which is an aromatic amine with a hydroxyl group attached to the phenyl ring.
6. Contains methylidene group

Explanation

The compound also has a methylidene functional group, which is a carbon-carbon double bond with two hydrogen atoms attached to the carbon atoms.
7. Used in research and experimental studies

Explanation

The compound is utilized in various scientific research and experimental studies, particularly in the fields of pharmaceutical research, material science, and organic synthesis.
8. Potential biological and pharmacological activities

Explanation

The compound may possess biological and pharmacological properties that could be beneficial in the development of new drugs or therapies.
9. Further studies being conducted

Explanation

Ongoing research is being carried out to explore the compound's potential uses and applications in various fields, including its possible role in drug development and other scientific areas.

Chemical structure

1-[(4-hydroxyphenyl)amino]methylidenenaphthalen-2(1H)-one

Check Digit Verification of cas no

The CAS Registry Mumber 894-96-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 894-96:
(5*8)+(4*9)+(3*4)+(2*9)+(1*6)=112
112 % 10 = 2
So 894-96-2 is a valid CAS Registry Number.

894-96-2SDS

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 (1Z)-1-[(4-hydroxyanilino)methylidene]naphthalen-2-one

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-[1]naphthaldehyd-(4-hydroxy-phenylimin)

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:894-96-2 SDS

894-96-2Relevant academic research and scientific papers

Synthesis, structure-activity relationships and preliminary mechanism study of N-benzylideneaniline derivatives as potential TLR2 inhibitors

Cai, Shaoyi,Zhu, Gengzheng,Cen, Xiaohong,Bi, Jingjie,Zhang, Jingru,Tang, Xiaoshan,Chen, Kun,Cheng, Kui

, p. 2041 - 2050 (2018/03/13)

Toll-like receptor 2 (TLR2) can recognize pathogen-associated molecular patterns to defense against invading organisms and has been represents an attractive therapeutic target. Until today, none TLR2 small molecule antagonist have been developed in clinic

Synthesis, characterization, and reactivity of Pd(II) salicylaldimine complexes derived from aminophenols

Tardiff, Bennett J.,Smith, Joshua C.,Duffy, Stephen J.,Vogels, Christopher M.,Decken, Andreas,Westcott, Stephen A.

, p. 392 - 399 (2008/03/15)

Schiff bases, derived from the condensation of salicylaldehydes with 3- and 4-aminophenol, reacted with palladium(II) acetate to give the corresponding bis(N-arylsalicylaldiminato)palladium(II) complexes. These complexes have been found to be active catalysts for the Suzuki-Miyaura cross-coupling of aryl bromides and iodides with aryl boronic acids, using water as a solvent.

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