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2-bromo-N-carbamoyl-2-ethyl-butanamide

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Identification
Molecular formula
C7H13BrN2O2
CAS number
179688-29-0
IUPAC name
2-bromo-N-carbamoyl-2-ethyl-butanamide
State
State

At room temperature, 2-bromo-N-carbamoyl-2-ethyl-butanamide exists as a solid. It is an organic compound that is commonly used in various chemical synthesis applications.

Melting point (Celsius)
108.00
Melting point (Kelvin)
381.15
Boiling point (Celsius)
256.00
Boiling point (Kelvin)
529.15
General information
Molecular weight
238.09g/mol
Molar mass
238.0820g/mol
Density
1.4700g/cm3
Appearence

2-bromo-N-carbamoyl-2-ethyl-butanamide typically appears as a crystalline solid. The appearance can vary slightly based on purity and specific conditions, but it commonly forms white or off-white crystals.

Comment on solubility

Solubility of 2-bromo-N-carbamoyl-2-ethyl-butanamide

The compound 2-bromo-N-carbamoyl-2-ethyl-butanamide showcases interesting solubility characteristics that deserve attention. Generally, the solubility of a compound is influenced by its molecular structure, polarity, and intermolecular interactions. Here are some key points to consider:

  • Polarity: The presence of both a bromo group and a carbamoyl functional group enhances the polarity of this compound, suggesting potential for solubility in polar solvents.
  • Hydrogen Bonding: The amide functional group (–CONH2) allows for hydrogen bonding, which can significantly increase its solubility in water and other hydrogen-bonding solvents.
  • Hydrophobic Character: The ethyl group introduces hydrophobic characteristics, potentially decreasing solubility in polar solvents. This balance between hydrophobic and hydrophilic portions plays a crucial role in solubility behavior.

In summary, while 2-bromo-N-carbamoyl-2-ethyl-butanamide is expected to have moderate solubility in polar solvents due to its functionality, its actual solubility will ultimately depend on specific conditions such as temperature and solvent choice. As a general rule, **"like dissolves like,"** emphasizing the importance of matching solvent properties to the compound's structural features.

Interesting facts

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

2-bromo-N-carbamoyl-2-ethyl-butanamide is a fascinating compound that has garnered attention in various fields of research. Here are some compelling points to consider:

  • Pharmaceutical Potential: This compound is being explored for its potential therapeutic applications due to its unique structure, which may interact with biological targets in the body.
  • Synthetic Versatility: The presence of the bromo group allows for versatile reactions that can lead to the synthesis of more complex molecules, making it a valuable intermediate in organic chemistry.
  • Structure-Activity Relationship: Researchers are keen on studying how modifications to its structure can influence its biological activity, aiding in drug design and discovery.
  • Environmental Impact: Understanding the behavior of such compounds is crucial in assessing their environmental persistence and potential toxicity, especially since halogenated compounds can have significant ecological consequences.
  • Analytical Techniques: Investigating compounds like 2-bromo-N-carbamoyl-2-ethyl-butanamide often involves advanced analytical techniques such as NMR (Nuclear Magnetic Resonance) and HPLC (High-Performance Liquid Chromatography) to ensure purity and resolve structural characteristics.

In the words of renowned chemist Linus Pauling, “The best way to have a good idea is to have a lot of ideas.” Each research endeavor involving 2-bromo-N-carbamoyl-2-ethyl-butanamide contributes to our understanding of organic chemistry and its potentials.

As studies continue, it becomes clear that the interactions and properties of compounds like this one have far-reaching implications across multiple scientific disciplines.

Synonyms
CARBROMAL
77-65-6
Adalin
Diacid
Hoggar
(2-Bromo-2-ethylbutyryl)urea
Bromadal
Bromacetocarbamide
Bromodiethylacetylurea
Addisomnol
Dormiturin
Pianadalin
Planadalin
Fydalin
Karbromal
Kartryl
Nenesin
Parkosed
Pelidorm
2-bromo-N-carbamoyl-2-ethylbutanamide
Nyctal
Tildin
Uradal
Bromdiethylacetylurea
Mirfudorm
Persomnin
Servadorm
Thalambrol
Somben
Bromodiethylacetylcarbamide
Bromacetocarbamidum
Carbromalum
Bromadel
Butanamide, N-(aminocarbonyl)-2-bromo-2-ethyl-
1-Bromo-ethyl-butyryl-urea
Carbromalum [INN-Latin]
2-Bromo-2-ethylbutyrylurea
NCI-C03805
Urea, (2-bromo-2-ethylbutyryl)-
CCRIS 124
2-Brom-2-ethylbutyrylmocovina
NSC 49191
N-(Aminocarbonyl)-2-bromo-2-ethylbutanamide
Adisomnol
HSDB 4100
(2-Brom-2-ethylbutyryl)harnstoff
2-bromo-2-ethylbutyryurea
EINECS 201-046-6
Carbromal (INN)
NSC-49191
UNII-0Y299JY9V3
2-Brom-2-ethylbutyrylmocovina [Czech]
BRN 1775637
Carbromal [INN:BAN:DCF:NF]
DTXSID8020252
AI3-51262
Carbrital (Salt/Mix)
0Y299JY9V3
CARBROMAL [INN]
CARBROMAL [MI]
CARBROMAL [HSDB]
CARBROMAL [MART.]
CARBROMAL [WHO-DD]
DTXCID80252
Urea, (2-bromo-ethylbutyryl)-
.alpha.-Bromo-.alpha.-ethylbutyrylurea
(.alpha.-Bromo-.alpha.-ethylbutyryl)urea
(.alpha.-Ethyl-.alpha.-bromobutyryl)urea
Carbromalum (INN-Latin)
Butanamide, N-aminocarbonyl-2-bromo-2-ethyl-
CARBROMAL (MART.)
(.alpha.-Bromo-.alpha.-ethylbutyryl)carbamide
Adalin; Adisomnol; Bromacetocarbamide; Bromadal
WLN: ZVMVXE2&2
.alpha.-Ethyl-.alpha.-bromobutyrylurea
alpha-Ethyl-alpha-bromobutyrylurea
(alpha-Bromo-alpha-ethylbutyryl)urea
(alpha-Bromo-alpha-ethylbutyryl)carbamide
Adalin (TN)
SCHEMBL261
(2-bromo-2-ethylbutanoyl)urea
CHEMBL1697828
N05CM04
NSC9916
CHEBI:134961
N-(2-Bromo-2-ethylbutanoyl)urea
ALBB-036461
HY-B1594
NSC-9916
NSC49191
(alpha-Ethyl-alpha-bromobutyryl)urea
Tox21_302247
N-(2-Bromo-2-ethylbutanoyl)urea #
AKOS027383909
DB13817
CAS-77-65-6
ALPHA-BROMO-ALPHA-ETHYLBUTYRYLUREA
NCGC00255200-01
(ALPHA-BROMO-ALPHA-ETHYLBUTYRL)UREA
DB-056237
CS-0013511
NS00003897
D02619
Q382185
SR-01000883968
SR-01000883968-1
N-(AMINOCARBONYL)-2-BROMO-2-ETHYL-BUTANAMIDE
201-046-6