304-11-0

Basic information

• Product Name: 1-(2,2-diphenylethenyl)-3-fluorobenzene
• CAS NO: 304-11-0
• Molecular Formula: C₂₀H₁₅F
• Molecular Weight: 274.3315
• Mol File: 304-11-0.mol

Chemical Properties

• Boiling Point: 358.2°C at 760 mmHg
• Flash Point: 188.7°C
• Density: 1.127g/cm³
• Vapor Pressure: 5.35E-05mmHg at 25°C
• Refractive Index: 1.631
• CAS DataBase Reference: 1-(2,2-diphenylethenyl)-3-fluorobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,2-diphenylethenyl)-3-fluorobenzene(304-11-0)
• EPA Substance Registry System: 1-(2,2-diphenylethenyl)-3-fluorobenzene(304-11-0)

Safety Data

• Hazardous Substances Data: 304-11-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
1-(2,2-diphenylethenyl)-3-fluorobenzene is used as a building block in organic synthesis for its ability to contribute to the formation of more complex molecules. Its unique structure allows for various chemical reactions, making it a versatile component in creating a range of organic compounds.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, 1-(2,2-diphenylethenyl)-3-fluorobenzene is employed as a key intermediate in the synthesis of different medicinal compounds. Its incorporation can lead to the development of new drugs with potential therapeutic applications.
Used in Material Science:
1-(2,2-diphenylethenyl)-3-fluorobenzene's properties make it a candidate for use in material science, where it can be part of the development of new materials with specific optical, electronic, or mechanical properties.
Used as a Precursor for Synthesis:
1-(2,2-diphenylethenyl)-3-fluorobenzene serves as a precursor for the synthesis of a variety of organic compounds, contributing to the diversity of chemical products available for various applications.
Used in Imaging Agents and Dyes:
Leveraging its fluorescent properties, 1-(2,2-diphenylethenyl)-3-fluorobenzene is used in the development of imaging agents and dyes. These can be crucial in medical diagnostics, research, and other fields requiring high-contrast visualization techniques.

Upstream product

• 530-48-3 1,1-Diphenylethylene 
• 1073-06-9 3-fluorobromobenzene 
• 27329-60-8 diethyl (diphenylmethyl)phosphonate 
• 456-48-4 3-Fluorobenzaldehyde 
• 456-42-8 m-fluorobenzyl chloride 

Downstream Products

• 1159-51-9 1-Brom-1-(3-fluor-phenyl)-2,2-diphenyl-aethylen 

Relevant articles and documents

Electrochemical Aziridination by Alkene Activation Using a Sulfamate as the Nitrogen Source

The first direct aziridination of triaryl-substituted alkenes was achieved by means of an electrochemical process that could extend to multisubstituted styrenes. Specifically, hexafluoroisopropanol sulfamate was used as a nucleophilic nitrogen source. Mechanistic experiments suggest that this electrochemical process proceeds by stepwise formation of two C?N bonds through reactions between cationic carbon species and the sulfamate.

Direct arylation of alkenes with aryl iodides/bromides through an organocatalytic radical process

A radical addition: A KOtBu-complex-promoted radical arylation of polysubstituted alkenes with aryl iodides/bromides proceeds in high efficiency (see scheme). Benzofuran derivatives are also produced starting from readily available allyl 2-iodophenyl ethers. Copyright