25069-29-8

Basic information

• Product Name: 3-[4-(Diphenylamino)phenyl]propenoic acid
• Synonyms: 3-[4-(Diphenylamino)phenyl]propenoic acid;3-(4-(diphenylamino)phenyl)acrylic acid
• CAS NO: 25069-29-8
• Molecular Formula: C₂₁H₁₇NO₂
• Molecular Weight: 315.3652
• Mol File: 25069-29-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 508.8°Cat760mmHg
• Flash Point: 261.5°C
• Appearance: /
• Density: 1.23g/cm³
• Vapor Pressure: 3.56E-11mmHg at 25°C
• Refractive Index: 1.686
• PKA: -95.54±0.10(Predicted)
• CAS DataBase Reference: 3-[4-(Diphenylamino)phenyl]propenoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[4-(Diphenylamino)phenyl]propenoic acid(25069-29-8)
• EPA Substance Registry System: 3-[4-(Diphenylamino)phenyl]propenoic acid(25069-29-8)

Safety Data

• Hazardous Substances Data: 25069-29-8(Hazardous Substances Data)

Usage

Chemical structure

Consists of a 3-phenylprop-2-enoic acid backbone with a 4-diphenylamino substituent

Use in organic chemistry and pharmaceuticals

Due to potential biological activities and therapeutic properties

Studied effects

Anti-inflammatory, anti-cancer, and anti-diabetic

Potential as a building block

For the synthesis of novel drugs and bioactive compounds

Versatile and important molecule

In the development of new drugs and therapeutic agents

InChI:InChI=1/C21H17NO2/c23-21(24)16-13-17-11-14-20(15-12-17)22(18-7-3-1-4-8-18)19-9-5-2-6-10-19/h1-16H,(H,23,24)/b16-13+

Upstream product

• 141-82-2 malonic acid 
• 4181-05-9 4-(diphenylamino)benzaldehyde 

Relevant articles and documents

The self-aggregation of fluorophore-triphenylamine nanostructures with tunable luminescent properties: The effect of acidity and rare earth ions

A D-π-A type triphenylamine derivative 3-(4-(diphenylamino)phenyl) acrylic acid (abbreviated as L) is designed, synthesized and characterized by single crystal X-ray diffraction analysis. The self-aggregation of L nanostructures in different acidity aqueous solutions and/or under the guidance of rare earth (RE) ions is studied, along with the corresponding optical properties. In strong acidic conditions, L molecules self-assemble to form two dimensional nanostructures. While in neutral aqueous solutions, L tends to form nanorods. In the strong alkali environment, nanofibers were obtained. Moreover, in acidic conditions, the existence of Tm3+ induces the L molecules to self-aggregate into nanoplates. Flower-like six branched structures are observed when Yb3+ is used. The changed morphology leads to tunable linear optical properties.