50648-93-6

Basic information

• Product Name: MESO-1,2-BIS(4-FLUOROPHENYL)ETHYLENEDIAMINE
• Synonyms: MESO-1,2-BIS(4-FLUOROPHENYL)ETHYLENEDIAMINE;1,2-BIS(4-FLUOROPHENYL)ETHANE-1,2-DIAMINE;MESO-1,2-BIS(4-FLUOROPHENYL)ETHYLENE- DIAMINE, 98ù;1,2-Bis(4-fluorophenyl)-1,2-ethanediamine;1,2-Bis(4-fluorophenyl)ethylenediamine;meso-1,2-Bis(4-fluorophenyl)ethylenediamine,98%
• CAS NO: 50648-93-6
• Molecular Formula: C₁₄H₁₄F₂N₂
• Molecular Weight: 248.27
• Mol File: 50648-93-6.mol
• Article Data: 1

Chemical Properties

• Melting Point: 100-104 °C
• Boiling Point: 356.4°Cat760mmHg
• Flash Point: 161.8°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 2.93E-05mmHg at 25°C
• CAS DataBase Reference: MESO-1,2-BIS(4-FLUOROPHENYL)ETHYLENEDIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: MESO-1,2-BIS(4-FLUOROPHENYL)ETHYLENEDIAMINE(50648-93-6)
• EPA Substance Registry System: MESO-1,2-BIS(4-FLUOROPHENYL)ETHYLENEDIAMINE(50648-93-6)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 45-36/37/39-26
• Hazardous Substances Data: 50648-93-6(Hazardous Substances Data)

Usage

Description

MESO-1,2-BIS(4-FLUOROPHENYL)ETHYLENEDIAMINE, also known as (1R,2S)-1,2-Bis(4-fluorophenyl)ethane-1,2-diamine, is an off-white crystalline powder with unique chemical properties. It is a reagent that plays a significant role in the fluorometric determination of reducing sugars in body fluids, making it a valuable compound in the field of analytical chemistry and biochemistry.

Uses

Used in Analytical Chemistry:
MESO-1,2-BIS(4-FLUOROPHENYL)ETHYLENEDIAMINE is used as a reagent for the fluorometric determination of reducing sugars in body fluids. Its application is crucial for accurately measuring and analyzing the levels of reducing sugars, which are essential for understanding various biological processes and diagnosing certain medical conditions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, MESO-1,2-BIS(4-FLUOROPHENYL)ETHYLENEDIAMINE is used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential applications in treating a wide range of diseases.
Used in Chemical Synthesis:
MESO-1,2-BIS(4-FLUOROPHENYL)ETHYLENEDIAMINE is also used as a building block in the synthesis of complex organic molecules. Its versatile chemical properties make it a valuable component in the creation of new compounds with potential applications in various industries, including materials science, agrochemicals, and specialty chemicals.

InChI:InChI=1/C14H14F2N2/c15-11-5-1-9(2-6-11)13(17)14(18)10-3-7-12(16)8-4-10/h1-8,13-14H,17-18H2/p+2/t13-,14+

Upstream product

• 125448-81-9 1,2-Bis-(4-fluoro-phenyl)-N,N'-bis-[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-ethane-1,2-diamine 
• 1185877-05-7 meso-1,2-bis(4-fluorophenyl)ethylenediamine 
• 58520-50-6 C₂₈H₂₂F₂N₂O₂ 
• 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 

Downstream Products

• 1413934-28-7 2,2,2-trichloroethyl ((1R,2R)-2-benzamido-1,2-bis(4-fluorophenyl)ethyl)carbamate 
• 1413934-38-9 bis(2,2,2-trichloroethyl)((1R,2R)-1,2-bis(4-fluorophenyl)ethane-1,2-diyl)dicarbamate 

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(