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Butylcarbamate

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Identification
Molecular formula
C24H42N2O5
CAS number
118292-33-8
IUPAC name
2-[2-(2-butoxy-3-methoxy-phenyl)ethyl-[2-(butylcarbamoyloxy)ethyl]amino]ethyl N-butylcarbamate
State
State

At room temperature, 2-[2-(2-butoxy-3-methoxy-phenyl)ethyl-[2-(butylcarbamoyloxy)ethyl]amino]ethyl N-butylcarbamate is typically a liquid, though it can also appear as a low-melting solid.

Melting point (Celsius)
42.50
Melting point (Kelvin)
315.60
Boiling point (Celsius)
438.00
Boiling point (Kelvin)
711.00
General information
Molecular weight
434.61g/mol
Molar mass
434.6080g/mol
Density
1.0400g/cm3
Appearence

2-[2-(2-butoxy-3-methoxy-phenyl)ethyl-[2-(butylcarbamoyloxy)ethyl]amino]ethyl N-butylcarbamate is a colorless liquid or low-melting solid with a characteristic odor. It might appear as a clear and slightly viscous liquid or as a crystalline structure if it's in solid form.

Comment on solubility

Solubility of 2-[2-(2-butoxy-3-methoxy-phenyl)ethyl-[2-(butylcarbamoyloxy)ethyl]amino]ethyl N-butylcarbamate

The solubility of 2-[2-(2-butoxy-3-methoxy-phenyl)ethyl-[2-(butylcarbamoyloxy)ethyl]amino]ethyl N-butylcarbamate can be influenced by several factors:

  • Polarity: This compound contains both polar and non-polar groups, which can affect its interaction with solvents. Generally, compounds with polar functional groups tend to be more soluble in polar solvents like water.
  • Hydrogen Bonding: The presence of carbamate groups suggests that the compound has the potential to form hydrogen bonds, which may enhance its solubility in specific solvents.
  • Chain Length: The presence of butyl and butoxy groups may impart hydrophobic characteristics, potentially reducing solubility in polar solvents while increasing solubility in organic solvents.

In general, it can be anticipated that the solubility of this compound will vary significantly based on the solvent employed:

  • In non-polar solvents, it is likely to exhibit higher solubility due to the hydrophobic alkyl chains.
  • In polar solvents, its solubility may be limited but could be improved by selecting solvents that promote hydrogen bonding.

Given these considerations, understanding the environmental conditions and solvent properties is paramount when evaluating the solubility of this complex chemical compound.

Interesting facts

Interesting Facts about 2-[2-(2-butoxy-3-methoxy-phenyl)ethyl-[2-(butylcarbamoyloxy)ethyl]amino]ethyl N-butylcarbamate

This intriguing compound belongs to a class known as carbamates, which are esters or salts of carbamic acid. Their versatility in biological systems makes them essential in various applications, especially in pharmaceuticals. Here are some captivating aspects of this compound:

  • Complex Structure: The structure exhibits multiple functional groups, including a carbamate moiety and an aromatic ring, which contribute to its potential reactivity and interactions.
  • Biological Significance: Due to its structural features, compounds similar to this one are often explored for their roles in drug development and therapeutic interventions.
  • Pharmacological Potential: Research indicates that carbamates might influence neuronal activity, and this particular compound may serve as a lead for creating new medications targeting the nervous system.
  • Synthetic Pathways: The creation of this compound involves intricate organic synthesis techniques, which can include techniques such as amide coupling and nucleophilic substitution.
  • Structure-Activity Relationship: Compounds of this nature are often studied for their structure-activity relationships (SAR), providing insights into how small changes in structure can significantly impact biological activity.

In summary, the compound 2-[2-(2-butoxy-3-methoxy-phenyl)ethyl-[2-(butylcarbamoyloxy)ethyl]amino]ethyl N-butylcarbamate serves as a fascinating example of how complex organic molecules can have vast implications in science and medicine. As quoted by noted chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This compound embodies the spirit of discovery that drives chemical research forward.