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3-(ethoxycarbonylamino)propyl N-phenylcarbamate

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Identification
Molecular formula
C13H18N2O4
CAS number
.Not available in CAS registry.
IUPAC name
3-(ethoxycarbonylamino)propyl N-phenylcarbamate
State
State

At room temperature, 3-(ethoxycarbonylamino)propyl N-phenylcarbamate is typically a solid. It is stable under standard conditions, but like many organic compounds, should be stored in a cool, dry place to prevent degradation or reaction with moisture.

Melting point (Celsius)
98.50
Melting point (Kelvin)
371.65
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
279.31g/mol
Molar mass
279.3130g/mol
Density
1.1400g/cm3
Appearence

3-(Ethoxycarbonylamino)propyl N-phenylcarbamate appears as a colorless to pale yellow solid or crystalline powder. It may take the form of fine, small crystals and usually has low solubility in water. The appearance can vary slightly depending on its purity and the specific conditions under which it has been stored or synthesized.

Comment on solubility

Solubility of 3-(ethoxycarbonylamino)propyl N-phenylcarbamate

The solubility of 3-(ethoxycarbonylamino)propyl N-phenylcarbamate can be considered from various perspectives:

  • Polarity: This compound contains both hydrophilic (ethoxy and amino groups) and hydrophobic (phenyl group) segments, which may influence its solubility in different solvents.
  • Solvent Interaction: It is likely to exhibit varying degrees of solubility in:
    • Apolar Solvents: May be less soluble due to the hydrophilic nature of the amine and carbonyl groups.
    • Polar Solvents: Likely more soluble, especially in water and alcohols, where hydrogen bonding can facilitate dissolution.
  • pH Dependence: The solubility might also change with pH, especially if it behaves as a weak acid or base.
  • Temperature Effects: Increased temperatures may enhance solubility, a common trait for many organic compounds.

In summary, the solubility behavior of 3-(ethoxycarbonylamino)propyl N-phenylcarbamate is a delicate balance determined by its molecular structure and the surrounding environment. As a rule of thumb, "like dissolves like," meaning this compound should show better solubility in solvents with similar polarities.

Interesting facts

Exploring 3-(ethoxycarbonylamino)propyl N-phenylcarbamate

3-(ethoxycarbonylamino)propyl N-phenylcarbamate is an intriguing compound with a variety of applications and attributes that may captivate any chemistry enthusiast. Known for its distinctive structural features, this compound is classified under the category of carbamates, which are esters or salts of carbamic acid. Here are some compelling facts about this compound:

  • Pharmacological Potential: The presence of the carbamate group suggests that this compound might exhibit biological activity, potentially as an antimicrobial or anti-inflammatory agent.
  • Synthesis and Reactions: The synthetic pathways to derive 3-(ethoxycarbonylamino)propyl N-phenylcarbamate often involve versatile reactions, including the N-acylation and esterification processes, which highlight the compound's adaptability in organic synthesis.
  • Applications in Agriculture: Given its structure, this compound may also have utility in agricultural chemistry, potentially serving as a precursor for developing herbicides or insecticides.
  • Research Interest: The unique characteristics of the compound keep it in the spotlight for organic chemistry research, where scientists are continually exploring its properties and interactions with other molecules.

As one delves deeper into the world of 3-(ethoxycarbonylamino)propyl N-phenylcarbamate, it becomes evident that this compound not only represents a fascinating chemical entity but also opens doors to potential advancements in both medicinal and agricultural fields. The exploration of its mechanisms, applications, and effects is sure to yield exciting findings in the future!

Synonyms
Ethyl (3-hydroxypropyl)carbamate carbanilate
BRN 2752042
CARBAMIC ACID, (3-HYDROXYPROPYL)-, ETHYL ESTER, CARBANILATE
5659-61-0
DTXSID10205140
DTXCID10127631