3172-38-1

Basic information

• Product Name: 1-{[(3-chlorophenyl)amino]methylidene}naphthalen-2(1H)-one
• CAS NO: 3172-38-1
• Molecular Formula: C₁₇H₁₂ClNO
• Molecular Weight: 281.7363
• Mol File: 3172-38-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 479.8°C at 760 mmHg
• Flash Point: 243.9°C
• Density: 1.39g/cm³
• Vapor Pressure: 2.3E-09mmHg at 25°C
• Refractive Index: 1.756
• CAS DataBase Reference: 1-{[(3-chlorophenyl)amino]methylidene}naphthalen-2(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-{[(3-chlorophenyl)amino]methylidene}naphthalen-2(1H)-one(3172-38-1)
• EPA Substance Registry System: 1-{[(3-chlorophenyl)amino]methylidene}naphthalen-2(1H)-one(3172-38-1)

Safety Data

• Hazardous Substances Data: 3172-38-1(Hazardous Substances Data)

Usage

Explanation

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

Explanation

The compound is derived from naphthalen-2(1H)-one, which is a type of aromatic ketone, and has a substituted aromatic amine group attached to it.

Explanation

This is another way to refer to the compound, highlighting the presence of a 3-chlorophenyl group and a benzylidene group.

Explanation

The compound is used in the synthesis of other organic compounds and is also utilized in the development of pharmaceuticals.

Explanation

The compound has been found to exhibit various biological activities, which could be useful in the development of new drugs and treatments.

Explanation

Due to its biological activities, the compound is being studied for its potential use in creating new medications and therapies for a range of diseases.

Explanation

The compound contains several functional groups, including an aromatic amine group, a carbonyl group, and a chloro substituent, which contribute to its chemical properties and reactivity.

Chemical structure

Naphthalen-2(1H)-one derivative with a substituted aromatic amine group and a carbonyl group

Industry applications

Organic synthesis and pharmaceutical industry

Biological activities

Antifungal, antibacterial, and antitumor properties

Potential use

Development of new drugs and treatments for various diseases

Functional groups

Aromatic amine, carbonyl, and chloro substituents

Upstream product

• 108-42-9 3-chloro-aniline 
• 708-06-5 2-hydroxynaphthalene-1-carbaldehyde 

Downstream Products

• 125727-43-7 VO(2-hydroxy-1-naphthalidene-3'-chloroaniline)2 

Relevant articles and documents

Potentiometric study of the lanthanide(III) ion complexes with some Schiff bases

The Schiff bases N-[2-hydroxy-1-naphthaledene]-3-substituted(R)-anilines (R = Cl, OCH3, CH3) have been synthesized. The stability constants of their complexes with lanthanide(III) ions have been determined at 30 ± 0.1° potentiometric