58520-50-6

Basic information

• Product Name: PHENOL, 2,2''-[[1,2-BIS(4-FLUOROPHENYL)1,2-ETHANEDIYL]BIS(NITRILOMETHYLIDYNE)]BIS-R,S
• Synonyms: PHENOL, 2,2''-[[1,2-BIS(4-FLUOROPHENYL)1,2-ETHANEDIYL]BIS(NITRILOMETHYLIDYNE)]BIS-R,S
• CAS NO: 58520-50-6
• Molecular Formula: C₂₈H₂₂F₂N₂O₂
• Molecular Weight: 456.48
• Mol File: 58520-50-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: PHENOL, 2,2''-[[1,2-BIS(4-FLUOROPHENYL)1,2-ETHANEDIYL]BIS(NITRILOMETHYLIDYNE)]BIS-R,S(CAS DataBase Reference)
• NIST Chemistry Reference: PHENOL, 2,2''-[[1,2-BIS(4-FLUOROPHENYL)1,2-ETHANEDIYL]BIS(NITRILOMETHYLIDYNE)]BIS-R,S(58520-50-6)
• EPA Substance Registry System: PHENOL, 2,2''-[[1,2-BIS(4-FLUOROPHENYL)1,2-ETHANEDIYL]BIS(NITRILOMETHYLIDYNE)]BIS-R,S(58520-50-6)

Safety Data

• Hazardous Substances Data: 58520-50-6(Hazardous Substances Data)

Usage

Description

PHENOL, 2,2''-[[1,2-BIS(4-FLUOROPHENYL)1,2-ETHANEDIYL]BIS(NITRILOMETHYLIDYNE)]BIS-R,S is a complex organic compound characterized by its unique molecular structure, which features a phenol core with fluorophenyl ethanediyl groups connected through nitrilmethylidine bridges. PHENOL, 2,2''-[[1,2-BIS(4-FLUOROPHENYL)1,2-ETHANEDIYL]BIS(NITRILOMETHYLIDYNE)]BIS-R,S is known for its potential applications in various fields due to its distinct chemical properties.

Uses

Used in Pharmaceutical Industry:
PHENOL, 2,2''-[[1,2-BIS(4-FLUOROPHENYL)1,2-ETHANEDIYL]BIS(NITRILOMETHYLIDYNE)]BIS-R,S is used as an intermediate in the synthesis of [1,2-bis(fluorophenylethylenediamine)platinum(II)] complexes. These complexes possess tumor-inhibiting properties, making them valuable in the development of anticancer drugs.
Used in Chemical Research:
PHENOL, 2,2''-[[1,2-BIS(4-FLUOROPHENYL)1,2-ETHANEDIYL]BIS(NITRILOMETHYLIDYNE)]BIS-R,S can also be utilized in chemical research as a starting material for the development of new molecules with potential applications in various fields, such as materials science, pharmaceuticals, and agrochemicals. Its unique structure allows for further functionalization and modification to explore new chemical properties and potential uses.

Upstream product

• 51208-45-8 meso-1,2-Bis-(2-hydroxyphenyl)ethylenediamine 
• 459-57-4 4-fluorobenzaldehyde 

Downstream Products

• 1185877-05-7 meso-1,2-bis(4-fluorophenyl)ethylenediamine 
• 90-02-8 salicylaldehyde 
• 50648-93-6 d,l-1,2-diamino-1,2-bis(4-fluorophenyl)ethane 
• 125448-81-9 1,2-Bis-(4-fluoro-phenyl)-N,N'-bis-[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-ethane-1,2-diamine 
• 125448-81-9 (1R,2R)-1,2-Bis-(4-fluoro-phenyl)-N,N'-bis-[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-ethane-1,2-diamine 

Relevant articles and documents

Tumor inhibiting platinum-(II) complexes. Part I: synthesis

The synthesis of the diastereomeric 1,2-bis(2-, 3-, and 4-fluorophenyl)ethylenediamines 4-6, 10-12 from meso-1,2-bis(2-hydroxyphenyl)ethylenediamine and 2-, 3-, and 4-fluorobenzaldehyde by a diaza-Cope-rearrangement and their conversion into the 1,2-bis(