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N,N-dibenzyl-3-chloropropan-1-amine

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Identification
Molecular formula
C17H20ClN
CAS number
774-48-1
IUPAC name
N,N-dibenzyl-3-chloro-propan-1-amine
State
State

At room temperature, N,N-dibenzyl-3-chloropropan-1-amine is typically in a liquid state.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
375.00
Boiling point (Kelvin)
648.15
General information
Molecular weight
273.80g/mol
Molar mass
273.8000g/mol
Density
1.0408g/cm3
Appearence

N,N-dibenzyl-3-chloropropan-1-amine typically appears as a colorless to pale yellow liquid. Its appearance may vary slightly depending on the purity and specific conditions under which it is stored.

Comment on solubility

Solubility of N,N-dibenzyl-3-chloro-propan-1-amine

N,N-dibenzyl-3-chloro-propan-1-amine, with its unique structure, exhibits interesting solubility characteristics. Generally, the solubility of this compound can be influenced by various factors:

  • Polarity: Due to the presence of the amine group, the molecule exhibits some polar character. However, the extensive benzyl groups contribute to its overall hydrophobic nature.
  • Solvent Interaction: N,N-dibenzyl-3-chloro-propan-1-amine tends to be more soluble in organic solvents such as ethanol or acetone compared to water, making it a candidate for non-aqueous reactions.
  • Temperature Dependence: Like many organic compounds, its solubility may increase with temperature, which promotes molecular movement and solvent interaction.

In summary, while N,N-dibenzyl-3-chloro-propan-1-amine displays limited solubility in polar solvents such as water, it thrives in non-polar or less polar organic solvents. This characteristic can be crucial when considering the compound for various chemical applications or reactions.

Interesting facts

Interesting Facts about N,N-Dibenzyl-3-chloro-propan-1-amine

N,N-dibenzyl-3-chloro-propan-1-amine is a fascinating chemical compound with diverse applications in organic synthesis and medicinal chemistry. As a member of the amine family, it exhibits properties that make it particularly valuable in research and industry.

Key Characteristics:

  • Amine Structure: This compound features two benzyl groups attached to a propan-1-amine backbone, enhancing its reactivity and stability.
  • Chlorination: The presence of a chlorine atom on the propan-1-amine enhances its electrophilic character, making it a useful intermediate in synthetic pathways.
  • Uses in Synthesis: N,N-dibenzyl-3-chloro-propan-1-amine can be utilized to create more complex molecules, aiding in the development of pharmaceuticals and agrochemicals.

One of the most intriguing aspects of this compound is its ability to act as a precursor for other important pharmaceuticals. As noted by researchers, "The functionalization of amines leads to a plethora of biologically active compounds." This highlights the significance of compounds like N,N-dibenzyl-3-chloro-propan-1-amine in drug development.

Applications:

  • Organic Synthesis
  • Pharmaceutical Development
  • Research in Biochemistry

In summary, N,N-dibenzyl-3-chloro-propan-1-amine holds a prominent position in the realm of organic chemistry, thanks to its unique structure and reactivity. Its ability to be transformed into useful compounds showcases the intricate connection between chemistry and the development of life-saving medicines.

Synonyms
N,N-dibenzyl-3-chloropropan-1-amine
16045-94-6
N,N-dibenzyl-3-chloro-1-propanamine
Benzenemethanamine, N-(3-chloropropyl)-N-(phenylmethyl)-
SCHEMBL6947716
DTXSID30274611
LHJJKBNOKYQDFO-UHFFFAOYSA-N
(N,N-dibenzylamino]-1-propylchloride
AKOS005267203
SB81767