3230-46-4

Basic information

• Product Name: 2-{[(E)-(4-bromophenyl)methylidene]amino}phenol
• CAS NO: 3230-46-4
• Molecular Formula: C₁₃H₁₀BrNO
• Molecular Weight: 276.1286
• Mol File: 3230-46-4.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 412.9°C at 760 mmHg
• Flash Point: 203.5°C
• Density: 1.38g/cm³
• Vapor Pressure: 2.09E-07mmHg at 25°C
• Refractive Index: 1.606
• CAS DataBase Reference: 2-{[(E)-(4-bromophenyl)methylidene]amino}phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{[(E)-(4-bromophenyl)methylidene]amino}phenol(3230-46-4)
• EPA Substance Registry System: 2-{[(E)-(4-bromophenyl)methylidene]amino}phenol(3230-46-4)

Safety Data

• Hazardous Substances Data: 3230-46-4(Hazardous Substances Data)

Usage

Structure

Contains a benzene ring with a bromine atom, an amino group, and a hydroxyl group attached

Type

Synthetic organic compound

Usage

Commonly used in laboratory research and pharmaceutical applications due to potential biological activity

Properties

Possesses antioxidant properties and may have potential therapeutic use

Handling and storage

Should be handled with care and stored in a cool, dry place away from heat and direct sunlight.

Upstream product

• 1122-91-4 4-bromo-benzaldehyde 
• 95-55-6 2-amino-phenol 

Downstream Products

• 17064-45-8 2-(4-biphenylyl)benzoxazole 

Relevant articles and documents

Tertiary amine derivatives and organic electroluminescent device including the same

A UV-region high-energy external light source is effectively absorbed to minimize damage to organic materials in the organic electroluminescent device. 1 Is a cross-sectional view of an organic electroluminescence device according to the present invention. O-2 electrode 1 Or more organic material layers disposed between the (2) and (1) th electrodes. A capping layer is included. The organic material layer and/or the capping layer may include the 1 st amine derivative represented by Formula 3. Chemical Formula 1. Wherein each substituent in Formula 1 is as defined in the description of the invention.

Enantioselective Strecker and Allylation Reactions with Aldimines Catalyzed by Chiral Oxazaborolidinium Ions

Chiral oxazaborolidinium ion (COBI)-catalyzed enantioselective nucleophilic addition reactions of aldimines using tributyltin cyanide and allyltributylstannane have been developed. Various α-aminonitriles and homoallylic amines were synthesized in high yi

Tertiary amine derivatives and organic electroluminescent device including the same

Provided is a tertiary amine derivative which contributes to a substantial increase in service life of an organic electroluminescent device by minimizing damages to organic matter inside the organic electroluminescent device via effective absorption of a high-energy external light source in the UV region. According to the present invention, the organic electroluminescent device comprises: a first electrode and a second electrode; and one or more organic material layers disposed between the first electrode and the second electrode, wherein the organic material layers comprise a tertiary amine derivative represented by chemical formula 1. In the chemical formula 1, Z_1, Z_2, and Z_3 are each independently O or S.COPYRIGHT KIPO 2020