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2-bromo-N-carbamoyl-3-methylbutanamide

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Identification
Molecular formula
C6H11BrN2O2
CAS number
50910-55-9
IUPAC name
2-bromo-N-carbamoyl-3-methyl-butanamide
State
State

At room temperature, 2-bromo-N-carbamoyl-3-methylbutanamide is typically a crystalline solid.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.15
Boiling point (Celsius)
175.00
Boiling point (Kelvin)
448.15
General information
Molecular weight
223.07g/mol
Molar mass
223.0730g/mol
Density
1.3680g/cm3
Appearence

2-bromo-N-carbamoyl-3-methylbutanamide appears as a white to off-white crystalline solid.

Comment on solubility

Solubility of 2-bromo-N-carbamoyl-3-methyl-butanamide

The solubility of 2-bromo-N-carbamoyl-3-methyl-butanamide (C6H11BrN2O2) can be evaluated considering several factors:

  • Polarity: The presence of a carbonyl group and nitrogen suggests a degree of polarity, which may enhance solubility in polar solvents.
  • Hydrogen Bonding: The amide functional group can participate in hydrogen bonding, further influencing solubility.
  • Hydrophobic Interactions: The alkyl chain provides a hydrophobic region that may reduce solubility in highly polar solvents.

In general, one might expect that:

  • It is likely soluble in polar organic solvents such as ethanol and methanol.
  • Its solubility in water may be limited but could improve with temperature due to increased kinetic energy.
  • Isolated studies might indicate different solubility behavior based on solvent choice.

In conclusion, while detailed experimental data would ultimately dictate the precise solubility characteristics of this compound, initial predictions based on its molecular structure suggest a moderate solubility profile in certain solvents. As with many organic compounds, solubility characterization can be nuanced and warrants individual investigation.

Interesting facts

Interesting Facts about 2-bromo-N-carbamoyl-3-methyl-butanamide

2-bromo-N-carbamoyl-3-methyl-butanamide is a fascinating compound that falls into the category of organic compounds featuring unique structural characteristics. Here are some intriguing points about this compound:

  • Structural Diversity: The presence of bromine in its structure not only adds a halogen element but also imparts distinct reactivity to the compound, which can be utilized in various chemical synthesis processes.
  • Potential Biological Application: Compounds similar to 2-bromo-N-carbamoyl-3-methyl-butanamide are often explored in pharmaceutical research. Their ability to interact with biological systems makes them candidates for drug development.
  • Carbamoyl Group: The carbamoyl group (-C(=O)NH2) is a key functional moiety that enhances the compound’s potential interactions with enzymes and proteins, which is vital in the context of medicinal chemistry.
  • Synthetic Pathways: The synthesis of this compound typically involves several steps, showcasing the importance of organic synthesis techniques. Mastery of these techniques is crucial for chemists working in laboratories.
  • Analytical Methods: Analyzing compounds like 2-bromo-N-carbamoyl-3-methyl-butanamide involves techniques such as NMR and mass spectrometry, helping scientists to confirm their structure and purity.

In summary, 2-bromo-N-carbamoyl-3-methyl-butanamide represents a rich field of study for chemists. Its diverse applications, structural features, and relevance in organic synthesis make it a noteworthy compound in the realm of chemical science!

Synonyms
Bromisoval
496-67-3
bromisovalum
bromovalerylurea
Bromvalerylurea
Bromural
Bromvaletone
Brovarin
Calmotin
Dagrabromyl
Dibroluur
Dormigene
Uvaleral
1-(2-Bromoisovaleryl)urea
2-bromo-N-carbamoyl-3-methylbutanamide
Upiol
Bromcarbamide
Bromocarbamide
Bromaral
Bromizoval
Alural
Bromisovalerylurea
2-Bromo-3-methylbutyrylurea
Bromovalerocarbamide
Bromvaletonum
Bromvalurea
Brovalurea
Abroval
Alluval
Bromoval
Bromoxil
Bromuvan
Brovalin
Isobromyl
Pivadorm
Pivadorn
Somnurol
Bromisoval [INN]
Butanamide, N-(aminocarbonyl)-2-bromo-3-methyl-
Bromvalerocarbamidum
2-Monobromoisovalerylurea
Monobromoisolvalerylurea
2-Bromisovalerylmocovina
alpha-Bromoisovaleroylurea
.alpha.-Bromisovalerylurea
Bromisovalum [INN-Latin]
(alpha-Bromoisovaleryl)urea
Bromovaluree
Bromvalerylurea [JAN]
alpha-Bromoisovaleric acid ureide
2-Bromisovalerylmocovina [Czech]
EINECS 207-825-7
alpha-Bromo-beta-dimethylpropanoylurea
N-(Aminocarbonyl)-2-bromo-3-methylbutanamide
Bromisoval (INN)
Bromural (TN)
Brovarin (TN)
Bromisovalum [NF]
BRN 1773255
Monobromoisovalerylurea
(2-bromo-3-methylbutanoyl)urea
66101-52-8
DTXSID2040656
Bromovalerylurea (TN)
UREA, (2-BROMO-3-METHYLBUTYRYL)-
.alpha.-Bromoisovaleric acid ureide
BROMISOVALUM [MI]
469GW8R486
BROMISOVAL [MART.]
BROMISOVAL [WHO-DD]
2-bromo-N-carbamoyl-3-methyl-butanamide
BROMOVALERYLUREA [JAN]
DTXCID0020656
CHEBI:77043
3-03-00-00123 (Beilstein Handbook Reference)
NCGC00160445-01
NCGC00160445-02
Bromoisovalum
Bromisovalum (INN-Latin)
BROMISOVAL (MART.)
.ALPHA.-BROMO-.BETA.-DIMETHYLPROPANOYLUREA
C6H11BrN2O2
Bromyl
Bromovalcarbamide
Bromovaleroylurea
Bromoisovalerylurea
CAS-496-67-3
B.V.U.
UNII-469GW8R486
MFCD00047873
Bromisoval (Standard)
alpha-Bromisovalerylurea
2-Bromo-isovaleryl urea
(.+/-.)-Bromisoval
Bromovalerylurea (JP17)
Bromovalerylurea (JP18)
1-(2-Bromisovaleryl)urea
(alpha-Bromoisovaleroyl)urea
(RS)-2-Bromoisovalerylurea
(.alpha.-Bromoisovaleryl)urea
SCHEMBL262870
(.alpha.-Bromoisovaleroyl)urea
CHEMBL1515611
SCHEMBL25366855
CHEBI:31304
HY-B2113R
N05CM03
HMS3886M19
N-(2-Bromo-3-methylbutanoyl)urea
BCP14648
HY-B2113
Tox21_111815
s5305
N-(2-Bromo-3-methylbutanoyl)urea #
AKOS001042611
Tox21_111815_1
CCG-266743
CS-7762
DB13370
FB38229
GS-3579
NCGC00160445-04
AC-32032
DB-071026
(alpha-bromo-beta,beta-dimethylpropanoyl)urea
B2842
NS00002006
EN300-06511
D01391
H10002
SBI-0653911.0001
AB01316119-02
Q420899
SR-01000040621
SR-01000040621-1
(.alpha.-Bromo-.beta.,.beta.-dimethylpropanoyl)urea
Z56895709
Butanamide, N-(aminocarbonyl)-2-bromo-3-methyl-, (+/-)-
207-825-7
Bromisovalum; Bromovalerylurea; 2-Bromo-N-Carbamoyl-3-Methyl-Butanamide; 2-Bromo-N-Carbamoyl-3-Methyl-Butyramide; N-Aminocarbonyl-2-Bromo-3-Methyl-Butanamide