1002339-79-8

Basic information

• Product Name: 1,2-Di(4-carboxyphenyl)-1,2-diphenylethylene
• Synonyms: 1,2-Di(4-carboxyphenyl)-1,2-diphenylethylene;4,4'-(1,2-Diphenylethene-1,2-diyl)dibenzoic acid;1,2-Di(4-carboxyphenyl)-1,2,2-triphenylethene;4,4'-(1,2-Diphenylvinyl)-1,2-di-(phenylcarboxylic acid)
• CAS NO: 1002339-79-8
• Molecular Formula: C₂₈H₂₀O₄
• Molecular Weight: 420.456
• Mol File: 1002339-79-8.mol

Chemical Properties

• Boiling Point: 587.1±50.0 °C(Predicted)
• Appearance: /
• Density: 1.271±0.06 g/cm3(Predicted)
• PKA: 3.82±0.10(Predicted)
• CAS DataBase Reference: 1,2-Di(4-carboxyphenyl)-1,2-diphenylethylene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Di(4-carboxyphenyl)-1,2-diphenylethylene(1002339-79-8)
• EPA Substance Registry System: 1,2-Di(4-carboxyphenyl)-1,2-diphenylethylene(1002339-79-8)

Safety Data

• Hazardous Substances Data: 1002339-79-8(Hazardous Substances Data)

Usage

Uses

Used in Chemical Synthesis:
1,2-Di(4-carboxyphenyl)-1,2-diphenylethylene is used as a building block for the synthesis of various organic compounds due to its reactive carboxyphenyl groups. These groups can easily undergo esterification with hydroxyl and amino groups, allowing for the creation of a wide range of molecules with diverse properties and applications.
Used in Fluorescent Materials:
As an AIE dye, 1,2-Di(4-carboxyphenyl)-1,2-diphenylethylene is used in the development of fluorescent materials for various applications, such as sensors, imaging, and optoelectronic devices. Its unique property of emitting light upon aggregation makes it an attractive choice for creating materials with enhanced fluorescence properties.
Used in Drug Delivery Systems:
1,2-Di(4-carboxyphenyl)-1,2-diphenylethylene can be utilized in the design of drug delivery systems, particularly for targeted drug delivery. Its ability to form aggregates and interact with other molecules through esterification can be exploited to create drug carriers with improved targeting and release properties.
Used in Analytical Chemistry:
The AIE properties of 1,2-Di(4-carboxyphenyl)-1,2-diphenylethylene make it a valuable tool in analytical chemistry for the detection and quantification of various analytes. Its fluorescence can be modulated in response to specific interactions, allowing for the development of highly sensitive and selective assays.
Used in Environmental Applications:
1,2-Di(4-carboxyphenyl)-1,2-diphenylethylene can be employed in environmental applications, such as the detection and removal of pollutants. Its AIE properties and ability to interact with other molecules through esterification can be utilized to create materials that selectively bind and remove contaminants from the environment.

Upstream product

• 78024-99-4 C₂₈H₁₈N₂ 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 
• 124-38-9 carbon dioxide 
• 184239-35-8 1,2-bis(4-bromophenyl)-1,2-diphenylethylene 

Relevant articles and documents

A new luminescent metal-organic framework based on dicarboxyl-substituted tetraphenylethene for efficient detection of nitro-containing explosives and antibiotics in aqueous media

In this work, we synthesized a dicarboxyl-substituted tetraphenylethene (TPE) ligand, 4,4′-(1,2-diphenylethene-1,2-diyl)dibenzoic acid (H2BCTPE), with a prominent aggregation-induced emission (AIE) feature. A two-fold interpenetrated luminescen

Fluorometric sensing of biogenic amines with aggregation-induced emission-active tetraphenylethenes

A fluorometric sensor for detection and identification of biogenic amines with carboxylic acid modified tetraphenylethenes (TPEs) based on aggregation-induced emission (AIE) is reported. A mixture of the carboxylic acid substituted TPE and biogenic amines