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1,2-Ethanediamine, N,N'-bis(4-fluorophenyl)-1,2-diphenyl- is a complex organic compound with the chemical formula C20H18F2N2. It is a derivative of 1,2-ethanediamine, featuring two 4-fluorophenyl groups attached to the nitrogen atoms and two phenyl groups attached to the carbon atoms. 1,2-Ethanediamine, N,N'-bis(4-fluorophenyl)-1,2-diphenyl- is characterized by its symmetrical structure and the presence of fluorine atoms, which can influence its reactivity and physical properties. It is typically used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and potential to form stable complexes with metal ions. The compound's properties, such as its solubility and stability, can be tailored for specific applications through the introduction of fluorine atoms, which can affect its electronic and steric characteristics.

2951-40-8

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2951-40-8 Usage

Functional Groups

Two amino groups (-NH2)
Two phenyl rings (C6H5)
Two 4-fluorophenyl groups (C6H4F)

Structure

The compound consists of a central methane (CH4) carbon atom, with two phenyl rings and two 4-fluorophenyl groups attached to the 1,2-positions of the methane carbon. Each of the phenyl rings is connected to an amino group.

Applications

Synthesis of pharmaceuticals
Synthesis of agrochemicals
Intermediate for organic synthesis

Reactivity

Versatile due to the presence of multiple functional groups and aromatic rings

Physical State

Likely a solid at room temperature, based on its molecular weight and structure

Solubility

Soluble in organic solvents such as ethanol, methanol, and dichloromethane

Stability

Stable under normal conditions, but may be sensitive to heat, light, or moisture

Hazards

Potential irritant or toxic if ingested, inhaled, or absorbed through the skin

Storage

Should be stored in a cool, dry, and well-ventilated area, away from heat and light sources

Safety Precautions

Use appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat when handling 1,2-Ethanediamine, N,N'-bis(4-fluorophenyl)-1,2-diphenyl-

Environmental Impact

Potentially harmful to aquatic life and should be disposed of according to local regulations

Synonyms

N,N'-Bis(4-fluorophenyl)-1,2-diphenylethane-1,2-diamine, 4,4'-Difluorobis(benzeneaminato)diphenylmethane

Check Digit Verification of cas no

The CAS Registry Mumber 2951-40-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,5 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2951-40:
(6*2)+(5*9)+(4*5)+(3*1)+(2*4)+(1*0)=88
88 % 10 = 8
So 2951-40-8 is a valid CAS Registry Number.

2951-40-8Downstream Products

2951-40-8Relevant academic research and scientific papers

Highly chemoselective crossed imino pinacol coupling reaction using the synergetic effect of boron trifluoride etherate and trichloromethylsilane

Shimizu, Makoto,Suzuki, Ikuhiro,Makino, Hiroaki

, p. 1635 - 1638 (2007/10/03)

Use of boron trifluoride etherate and trichloromethylsilane in the presence of zinc-copper couple effects a crossed imino pinacol coupling reaction to give 1,2-diamines in good yields with high diastereoselectivities.

Organic reaction in water. Part 1. A convenient method for reduction of imines using zinc powder

Tsukinoki, Takehito,Mitoma, Yoshiharu,Nagashima, Satoko,Kawaji, Takatoshi,Hashimoto, Iwao,Tashiro, Masashi

, p. 8873 - 8876 (2007/10/03)

Reduction of imines was performed with zinc powder in 5% aqNaOH solution without any organic solvents under mild conditions, and the corresponding amines were obtained in good yields.

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