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Fenobucarb

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Identification
Molecular formula
C12H17NO3
CAS number
3766-81-2
IUPAC name
[3-(butanoylamino)phenyl] N-methylcarbamate
State
State

Solid at room temperature.

Melting point (Celsius)
70.00
Melting point (Kelvin)
343.15
Boiling point (Celsius)
383.00
Boiling point (Kelvin)
656.15
General information
Molecular weight
207.24g/mol
Molar mass
207.2440g/mol
Density
1.1470g/cm3
Appearence

Fenobucarb appears as a white to pale yellow crystalline powder. It is typically odorless.

Comment on solubility

Solubility of [3-(butanoylamino)phenyl] N-methylcarbamate

The solubility characteristics of the compound [3-(butanoylamino)phenyl] N-methylcarbamate are quite intriguing. This compound, like many others, demonstrates varying solubility profiles depending on the solvent used. Here are some key points regarding its solubility:

  • Polar Solvents: This compound tends to exhibit good solubility in polar solvents such as water and alcohols. The presence of functional groups such as amines and carbamates enhances its ability to interact with polar molecules.
  • Non-Polar Solvents: Conversely, its solubility in non-polar solvents like hydrocarbons is typically low. This is due to the significant ionic and polar interactions present within the molecule.
  • pH Dependence: The solubility may also change with pH, especially if there are ionizable groups. This can lead to increased solubility in alkaline or acidic conditions where protonation or deprotonation occurs.
  • Temperature Sensitivity: Temperature can significantly affect solubility; many compounds show increased solubility at elevated temperatures.

In summary, while [3-(butanoylamino)phenyl] N-methylcarbamate is generally soluble in polar solvents, its solubility behavior is contingent upon various factors such as solvent type, pH, and temperature. Understanding these factors is essential for applications in pharmaceuticals and organic synthesis, where solubility can be critical for the functionality of the compound.

Interesting facts

Interesting Facts about [3-(butanoylamino)phenyl] N-methylcarbamate

[3-(butanoylamino)phenyl] N-methylcarbamate is an intriguing compound that blends organic chemistry with medicinal applications. Here are some fascinating insights into its structure and uses:

  • Unique Structure: This compound features a phenyl ring substituted with a butanoylamino group, highlighting the versatility of amine functionalities in organic synthesis.
  • Carbamate Moiety: The presence of a carbamate functional group is significant, as it is frequently encountered in pharmaceuticals and agrochemicals, providing a linkage that enhances compound stability.
  • Biological Activity: Compounds like this one can exhibit diverse biological properties, making them potential candidates in drug discovery, particularly in the development of agrochemicals and therapeutic agents.
  • Synthesis Routes: The synthetic pathways to obtain this compound often involve nucleophilic substitutions or acylation reactions which are foundational concepts in organic chemistry.
  • Research Relevance: The exploration of compounds with similar structures contributes to the understanding of structure-activity relationships (SAR), crucial for tailoring compounds with desired bioactivity.

In summary, [3-(butanoylamino)phenyl] N-methylcarbamate is not just a compound of theoretical interest; it embodies a crucial intersection of chemistry and biology, representing how small changes in chemical structure can lead to significant variations in functionality. As highlighted by renowned chemist Robert H. Grubbs, "Chemistry is the study of matter, but I prefer to view it as the study of change." This compound exemplifies that change in action.

Synonyms
17814-27-6
Stauffer R 12466
m-Butyramidophenyl methylcarbamate
[3-(butanoylamino)phenyl] N-methylcarbamate
3'-(Methylcarbamoyloxy)butyranilide
Y2U3UWS0O3
NSC-222514
Butanamide, N-(3-(((methylamino)carbonyl)oxy)phenyl)-
BUTYRANILIDE, 3'-HYDROXY-, METHYLCARBAMATE (ester)
N-[3-(Methylcarbamoyloxy)phenyl]butyramide
3'-Hydroxybutranilide methylcarbamic acid ester
Butanamide, N-[3-[[(methylamino)carbonyl]oxy]phenyl]-
Carbamic acid, methyl-, ester with 3'-hydroxybutyranilide
R 12466
NSC 222514
BRN 2130852
AI3-27637
Butyranilide, 3'-hydroxy-, methylcarbamate
UNII-Y2U3UWS0O3
WLN: 3VMR COVM1
Butyranilide, methylcarbamate
R-12466
DTXSID30170427
Butanamide, N-(3-(((methylamino)carbonyl)oxy)phenyl)- (9CI)
NSC222514
[3-(Butanoylamino)phenyl]n-methylcarbamate
N-(3-(((METHYLAMINO)CARBONYL)OXY)PHENYL)BUTANAMIDE