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[3-(methoxycarbonylamino)phenyl] N-butylcarbamate

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Identification
Molecular formula
C14H20N2O4
CAS number
884497-99-6
IUPAC name
[3-(methoxycarbonylamino)phenyl] N-butylcarbamate
State
State

At room temperature, [3-(methoxycarbonylamino)phenyl] N-butylcarbamate is in a solid state typically characterized by its crystalline structure.

Melting point (Celsius)
78.50
Melting point (Kelvin)
351.65
Boiling point (Celsius)
397.50
Boiling point (Kelvin)
670.65
General information
Molecular weight
252.29g/mol
Molar mass
252.2880g/mol
Density
1.1200g/cm3
Appearence

[3-(methoxycarbonylamino)phenyl] N-butylcarbamate typically appears as a white crystalline solid. Its exact appearance might vary slightly depending on purity and environmental conditions.

Comment on solubility

Solubility of [3-(methoxycarbonylamino)phenyl] N-butylcarbamate

[3-(methoxycarbonylamino)phenyl] N-butylcarbamate is a chemical compound whose solubility can largely depend on various environmental factors and its chemical structure. Understanding its solubility is essential for practical applications, such as in formulations and synthesis processes.

Key Factors Affecting Solubility:

  • Polarity: The presence of polar functional groups, such as carbamate and methoxycarbonylamino, can enhance solubility in polar solvents.
  • Hydrogen Bonding: The compound may engage in hydrogen bonding with solvent molecules, further influencing solubility.
  • Temperature: Increased temperature typically enhances solubility for most compounds, making it an important consideration for experiments.
  • pH Level: The solubility may vary with pH changes, especially in biological systems or aqueous solutions.

In general, substances like [3-(methoxycarbonylamino)phenyl] N-butylcarbamate that contain both polar and nonpolar characteristics tend to exhibit variable solubility. It is often noted that "solubility is a merry dance of interactions." Hence, precise data regarding its solubility characteristics should be obtained through empirical testing to ensure reliable and accurate information for any intended use.

Interesting facts

Interesting Facts about [3-(methoxycarbonylamino)phenyl] N-butylcarbamate

[3-(methoxycarbonylamino)phenyl] N-butylcarbamate is a fascinating chemical compound that combines several functional groups, making it a subject of interest in both organic chemistry and medicinal applications. Here’s why this compound stands out:

  • Functional Versatility: This compound features an aromatic ring along with a carbamate and an amino group, exhibiting a wide range of reactivity. The carbamate group in particular is well-known for its biological significance and is commonly found in herbicides and pharmaceutical agents.
  • Medicinal Applications: Compounds with similar structures often have roles in drug design and development. By modifying the side chains, researchers can impact the biological activity significantly, making this compound a valuable candidate in pharmaceutical research.
  • Research Potential: The unique combination of the methoxycarbonyl and butylcarbamate groups may lead to innovative applications. For instance, it can be explored for its role in the synthesis of more complex molecules through various organic reactions.
  • Environmental Considerations: Carbamate derivatives can be biodegradable, which is a major advantage in reducing ecological impact. This has garnered attention for environmental chemistry studies, focusing on sustainable practices in chemical manufacturing.
  • Synthesis Pathways: The development of this compound is typically achieved through specific synthetic routes that allow for selective functionalization of the aromatic ring. This provides an excellent educational platform for students learning about reaction mechanisms and synthesis strategies.

In conclusion, [3-(methoxycarbonylamino)phenyl] N-butylcarbamate illustrates the intricate balance between functional design and biological utility, making it a compound of ongoing interest in scientific inquiry. Its versatility and potential applications show that deepening our understanding of its structure and properties can lead to exciting advancements in chemistry.

Synonyms
13684-36-1
CARBANILIC ACID, m-HYDROXY-, METHYL ESTER, BUTYLCARBAMATE (ester)
[3-(methoxycarbonylamino)phenyl] N-butylcarbamate
6PI9YJ1ZX0
NSC-222534
Carbamic acid, butyl-, 3-((methoxycarbonyl)amino)phenyl ester
Methyl N-(m-((butylcarbamoyl)oxy)phenyl)carbamate
NSC 222534
BRN 2419804
UNII-6PI9YJ1ZX0
WLN: 4MVOR CMVO1
DTXSID70159973
NSC222534
Carbanilic acid, methyl ester, butylcarbamate
NS00122506
[3-(Methoxycarbonylamino)phenyl]n-butylcarbamate
Carbamic acid, 3-[(methoxycarbonyl)amino]phenyl ester
METHYL N-(3-(N-BUTYLCARBAMOYLOXY)PHENYL)CARBAMATE