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N-(acetylcarbamoyl)-2-bromo-2-ethyl-butanamide

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Identification
Molecular formula
C9H15BrN2O3
CAS number
123456-78-9
IUPAC name
N-(acetylcarbamoyl)-2-bromo-2-ethyl-butanamide
State
State

At room temperature, N-(acetylcarbamoyl)-2-bromo-2-ethyl-butanamide is in a solid state. It is typically stored in a dry, stable environment to preserve its stability and prevent any degradation or reaction that could occur if exposed to moisture or heat.

Melting point (Celsius)
130.00
Melting point (Kelvin)
403.15
Boiling point (Celsius)
338.50
Boiling point (Kelvin)
611.65
General information
Molecular weight
251.14g/mol
Molar mass
251.0860g/mol
Density
1.3759g/cm3
Appearence

N-(acetylcarbamoyl)-2-bromo-2-ethyl-butanamide appears as a crystalline solid. The color can range from white to off-white.

Comment on solubility

Solubility of N-(acetylcarbamoyl)-2-bromo-2-ethyl-butanamide

N-(acetylcarbamoyl)-2-bromo-2-ethyl-butanamide possesses unique solubility characteristics that make it interesting within the context of chemical applications and formulations. Understanding its solubility helps in predicting its behavior in various solvents and environments.

Generally, the solubility of such amides can be influenced by a variety of factors:

  • Polarity: Due to the presence of polar groups like amide and acetyl, this compound shows a tendency to dissolve in polar solvents such as water and alcohols.
  • Hydrogen Bonding: The ability to form hydrogen bonds significantly enhances its solubility in aqueous solutions, particularly in water.
  • Solvent-Solute Interactions: The compatibility of the compound with the solvents can lead to increased solubility; for instance, it may dissolve well in solvents that can stabilize the polar features of the compound.
  • Temperature Effect: Like most organic compounds, higher temperatures could aid the solubility, allowing increased kinetic energy to facilitate solute-solvent interactions.

In summary, while N-(acetylcarbamoyl)-2-bromo-2-ethyl-butanamide is expected to be soluble in polar solvents, the exact solubility can vary widely based on the specific conditions and medium.

Interesting facts

Interesting Facts about N-(acetylcarbamoyl)-2-bromo-2-ethyl-butanamide

N-(acetylcarbamoyl)-2-bromo-2-ethyl-butanamide is a fascinating compound with unique characteristics that make it noteworthy in the field of chemistry. This compound belongs to a class known as amides, which are derivatives of carboxylic acids and exhibit a wide range of biological activities.

Biological Significance

  • Pharmaceutical Relevance: Amides are widely studied in drug development for their ability to influence biological pathways.
  • Potential Agrochemical Uses: Its structure suggests potential applications in enhancing agricultural yield or pest resistance.
  • Biochemical Interactions: Understanding its behavior helps in deciphering interactions with enzymes and receptors in biological systems.

Synthetic Pathways

The synthesis of N-(acetylcarbamoyl)-2-bromo-2-ethyl-butanamide showcases the creativity of synthetic chemistry:

  • Stepwise Synthesis: The production of this compound often involves multi-step synthetic routes, which can highlight various transformation techniques.
  • Use of Reagents: Key reagents used in its synthesis can vary, providing insight into reaction mechanisms and conditions.
  • Functionalization: The presence of bromine and acetyl groups provides opportunities for further chemical modifications.

Physical Chemistry Insights

Studying this compound can also lead to interesting discussions regarding:

  • Intermolecular Forces: The interactions between amides can significantly impact their properties and reactivity.
  • Quantum Chemistry: The exploration of its electronic structure helps in understanding its stability and reactivity.

In conclusion, N-(acetylcarbamoyl)-2-bromo-2-ethyl-butanamide not only represents a complex molecular structure but also serves as a gateway to various scientific explorations, from pharmaceutical applications to advanced synthetic methods. Its study can inspire chemists to further probe into the multifaceted nature of amides and their roles in both natural and synthetic systems.

Synonyms
Acecarbromal
77-66-7
Acetylcarbromal
Acetylbromodiethylacetylcarbamide
Paxarel
Abasin
Acetcarbromal
Sedamyl
Acetkarbromal
Carbased
Sedmynol
Adityl
Darolon
Ibatran
Sedtran
Absin
Acetyl adalin
Acecarbromal [INN]
N-Acetyl-N-bromodiethylacetylurea
1-Acetyl-3-(2-bromo-2-ethylbutyryl)urea
Butanamide, N-((acetylamino)carbonyl)-2-bromo-2-ethyl-
Butanamide, N-[(acetylamino)carbonyl]-2-bromo-2-ethyl-
N-(acetylcarbamoyl)-2-bromo-2-ethylbutanamide
E47C56IGOY
N-((Acetylamino)carbonyl)-2-bromo-2-ethylbutanamide
DTXSID9058810
Acecarbromal (INN)
UREA, 1-ACETYL-3-(2-BROMO-2-ETHYLBUTYRYL)-
Acetcarbromalum
1-Acetyl-3-(.alpha.-bromo-.alpha.-ethylbutyryl)urea
Acecarbromalum
Acetcarbromal; Acetyl Adalin; Acetylcarbromal; Adityl; Carbased; Darolon
Acecarbromalum [INN-Latin]
EINECS 201-047-1
N-Acetyl-N-bromodiethylacetylcarbamide
UNII-E47C56IGOY
BRN 1791982
1-Acetyl-3-(alpha-bromo-alpha-ethylbutyryl)urea
N-Acetyl-N'-alpha-bromo-alpha-ethylbutyrylcarbamide
Paxarel (TN)
ACECARBROMAL [MI]
ACECARBROMAL [MART.]
ACECARBROMAL [WHO-DD]
SCHEMBL600367
ACETYLCARBROMAL [VANDF]
CHEMBL2104673
DTXCID7047936
CHEBI:135155
N-Acetyl-N'-diethylbromoacetylurea
AKOS040750049
DB-056239
NS00005245
D07059
N-Acetyl-N'-(2-bromo-2-ethylbutanoyl)urea #
SR-01000883965
Q1113346
SR-01000883965-1
N-Acetyl-N'-.alpha.-bromo-.alpha.-ethylbutyrylcarbamide
N-(ACETYLAMINO)CARBONYL-2-BROMO-2-ETHYL-BUTANAMIDE
1-[(1Z)-2-bromo-2-ethyl-1-hydroxybutylidene]-3-[(1Z)-1-hydroxyethylidene]urea