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2-Bromo-2-ethylbutanamide

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Identification
Molecular formula
C6H12BrNO
CAS number
51568-46-8
IUPAC name
2-bromo-2-ethyl-butanamide
State
State

2-Bromo-2-ethylbutanamide is typically a solid at room temperature. Its crystalline structure allows for a stable formation, and it retains solidity under standard laboratory conditions.

Melting point (Celsius)
64.00
Melting point (Kelvin)
337.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
180.08g/mol
Molar mass
180.0450g/mol
Density
1.3190g/cm3
Appearence

2-Bromo-2-ethylbutanamide appears as a white to off-white crystalline solid. The crystals exhibit a sheen that is characteristic of many amide compounds, particularly those substituted with halogens, such as bromine in this case.

Comment on solubility

Solubility of 2-bromo-2-ethyl-butanamide

2-bromo-2-ethyl-butanamide, a compound with intriguing properties, exhibits notable characteristics regarding its solubility.

When discussing the solubility of this compound, consider the following points:

  • Polar Nature: The presence of the amide functional group makes 2-bromo-2-ethyl-butanamide polar. This enhances its ability to interact with polar solvents.
  • Solvent Compatibility: It is generally soluble in polar solvents such as water and alcohols due to hydrogen bonding capabilities.
  • Hydrophobic Elements: The alkyl side chain introduces hydrophobic characteristics, which can limit solubility in non-polar solvents.
  • Temperature Dependency: Solubility may vary with temperature; increasing temperature often improves solubility in liquids.

In summary, while 2-bromo-2-ethyl-butanamide is soluble in polar solvents due to its amide group, the hydrophobic nature brought by its alkyl components can create challenges in non-polar environments. Thus, it exemplifies the delicate balance between polar and non-polar interactions influencing solubility behavior.

Interesting facts

Interesting Facts about 2-bromo-2-ethyl-butanamide

2-bromo-2-ethyl-butanamide is a fascinating organic compound that falls within the category of amides. This compound is notable for its unique branching structure, which contributes to its diverse chemical behavior and potential applications.

Key Characteristics

  • Branching Structure: The presence of both bromine and ethyl groups on the butanamide skeleton enhances its reactivity, making it an interesting target for chemists looking to explore new reactions.
  • Biological Relevance: As an amide, it can potentially mimic biological molecules, opening avenues for research in medicinal chemistry, particularly in drug design.
  • Versatile Derivative: The bromine atom serves as a functional handle for further transformations, allowing chemists to create more complex molecular architectures.

Applications

Due to its unique properties, 2-bromo-2-ethyl-butanamide has the potential to be utilized in various fields such as:

  • Pharmaceutical Industry: Researchers may explore its properties to develop novel therapeutics.
  • Material Science: Its chemical structure could be tailored for use in polymers or specialized materials.

Quote to Ponder

"Chemistry is not about atoms, it is about the interactions between them." - Anon
This quote perfectly encapsulates the importance of understanding compounds like 2-bromo-2-ethyl-butanamide, as its interactions could lead to groundbreaking innovations.

Overall, 2-bromo-2-ethyl-butanamide stands as a testament to the intricate world of organic chemistry, urging chemists to delve deeper into its potential across various scientific disciplines.

Synonyms
2-Bromo-2-ethylbutyramide
Carbromide
Diethylbromoacetamide
2-Bromo-2-ethylbutanamide
UNII-6BTQ2OHW47
EINECS 208-132-2
6BTQ2OHW47
BRN 1751298
NSC-4607
2-Bromo-2-ethylbutylamide
DIETHYLBROMOACETAMIDE [MI]
DTXSID80199108
3-02-00-00755 (Beilstein Handbook Reference)
DTXCID70121599
aceyamoagudvaq-uhfffaoysa-n
Neuronal
Carabromide
511-70-6
2-Ethyl-2-bromobutyramide
2-Bromo-2,2-diethylacetamide
Butanamide, 2-bromo-2-ethyl-
BUTYRAMIDE, 2-BROMO-2-ETHYL-
NSC 4607
Bromdiathylacetamid
WLN: ZVXE2&2
SCHEMBL318239
NSC4607
NS00032224
Q27264457