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N,N-diethyl-N'-isopropyl-N'-phenyl-ethane-1,2-diamine

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Identification
Molecular formula
C15H26N2
CAS number
NA
IUPAC name
N,N-diethyl-N'-isopropyl-N'-phenyl-ethane-1,2-diamine
State
State

At room temperature, N,N-diethyl-N'-isopropyl-N'-phenyl-ethane-1,2-diamine is in a liquid state. This compound exhibits an oily consistency and is less dense than water.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
263.00
Boiling point (Kelvin)
536.15
General information
Molecular weight
220.36g/mol
Molar mass
220.3630g/mol
Density
0.8970g/cm3
Appearence

The compound is typically a colorless to pale yellow liquid with a characteristic amine-like odor. It is generally clear and may appear slightly viscous.

Comment on solubility

Solubility of N,N-Diethyl-N'-isopropyl-N'-phenyl-ethane-1,2-diamine

The solubility of N,N-diethyl-N'-isopropyl-N'-phenyl-ethane-1,2-diamine in various solvents provides intricate insights into its chemical behavior. This compound exhibits a relatively low solubility in water, primarily due to the large organic groups that hinder interaction with the polar water molecules. However, it demonstrates better solubility in non-polar and slightly polar organic solvents. Here are some key points about its solubility:

  • Low Aqueous Solubility: Its bulky organic structure does not favor solvation in water.
  • Solubility in Organic Solvents: It is more soluble in solvents like DMSO, ethanol, and chloroform, where the interactions between the solvent and solute are more favorable.
  • Hydrophobic Interactions: The hydrophobic nature of the ethyl, isopropyl, and phenyl groups plays a significant role in promoting solubility in non-polar environments.

In conclusion, the solubility characteristics of N,N-diethyl-N'-isopropyl-N'-phenyl-ethane-1,2-diamine highlight its preference for organic solvents over water, encapsulating the delicate balance between hydrophobic and polar molecule interactions.

Interesting facts

Exploring N,N-Diethyl-N'-isopropyl-N'-phenyl-ethane-1,2-diamine

N,N-Diethyl-N'-isopropyl-N'-phenyl-ethane-1,2-diamine is a fascinating compound known for its applications in various fields, particularly in organic synthesis and medicinal chemistry. Here are some intriguing facts that highlight its significance:

  • Versatile Building Block: This compound serves as a versatile intermediate in the synthesis of complex organic molecules, enabling chemists to create a variety of derivatives with unique properties.
  • Pharmacological Potential: With its amine functional groups, the compound may exhibit interesting biological activities, making it a candidate for potential pharmaceutical applications. As researchers explore its effects, it could lead to the development of new therapeutics.
  • Synthetic Pathways: Its structure allows for multiple synthetic strategies, such as alkylation and condensation reactions, which are vital for advancing the field of synthetic organic chemistry.
  • Chiral Centers: The chiral nature of certain isomers of this compound can lead to the production of enantiomerically pure substances, which are essential in the development of drugs that require a specific stereochemistry for efficacy.
  • Research Implications: Ongoing research into the reactivity and properties of N,N-diethyl-N'-isopropyl-N'-phenyl-ethane-1,2-diamine can yield insights into structure-activity relationships, guiding future experiments in molecular design.

In summary, the study of N,N-diethyl-N'-isopropyl-N'-phenyl-ethane-1,2-diamine not only enriches the understanding of chemical reactivity and synthesis but also opens the door to innovative medicinal applications. As synthetic chemists continue to explore the vast landscape of amines, this compound stands out as a key player in unraveling new possibilities in both industry and research.

Synonyms
ETHYLENEDIAMINE, N,N-DIETHYL-N'-ISOPROPYL-N'-PHENYL-
6248-17-5
1709 F
BRN 3287144
N,N-Diethyl-N'-isopropyl-N'-phenylethylenediamine
SCHEMBL10774772
DTXSID60211519