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Butabarbital

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Identification
Molecular formula
C10H16N2O3
CAS number
125-40-6
IUPAC name
5-allyl-5-sec-butyl-hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, butabarbital is in a solid state as a crystalline powder. It is stable under normal conditions and should be stored in a tightly closed container to prevent moisture absorption.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
226.28g/mol
Molar mass
226.2770g/mol
Density
1.0400g/cm3
Appearence

Butabarbital typically appears as a white crystalline powder. It is practically odorless and has a slightly bitter taste. The compound has a crystalline structure and can be processed into tablets or pills for medicinal use.

Comment on solubility

Solubility of 5-allyl-5-sec-butyl-hexahydropyrimidine-2,4,6-trione

The solubility of 5-allyl-5-sec-butyl-hexahydropyrimidine-2,4,6-trione can be influenced by several factors, making it an intriguing compound to study:

  • Polarity: The presence of both polar and nonpolar functional groups in this compound can lead to varied solubility in different solvents.
  • Hydrogen Bonding: The trione groups may engage in hydrogen bonding, which can enhance solubility in polar solvents like water.
  • Chain Length and Structure: The branched sec-butyl group and the allyl group might affect overall molecular interactions, potentially decreasing solubility in highly polar solvents.

In general, for compounds like this one, you may observe the following solubility characteristics:

  1. Biphasic Behavior: Possibility of being more soluble in organic solvents compared to aqueous solutions due to hydrophobic characteristics.
  2. Temperature Dependency: Changes in temperature could either increase or decrease solubility based on molecular interactions during solvation.
  3. Concentration Effects: Higher concentrations could lead to saturation thresholds, influencing solubility limits.

Ultimately, to determine the exact solubility of 5-allyl-5-sec-butyl-hexahydropyrimidine-2,4,6-trione, empirical measurements in different solvents are essential. It is always exciting to explore how diverse chemical structures interact with their environments!

Interesting facts

Interesting Facts about 5-allyl-5-sec-butyl-hexahydropyrimidine-2,4,6-trione

5-allyl-5-sec-butyl-hexahydropyrimidine-2,4,6-trione is a fascinating compound belonging to the class of pyrimidines, which are renowned for their diverse biological activities. Here are some intriguing aspects of this compound:

  • Versatile Chemical Structure: This compound features a complex structure that includes both an allyl group and a sec-butyl group. Such modifications can significantly influence its reactivity and biological properties.
  • Biological Relevance: Compounds containing pyrimidine rings are key players in many biochemical processes. They often serve as building blocks for nucleotides, which are essential for DNA and RNA structure.
  • Nutraceutical Potential: Some pyrimidine derivatives have been studied for their potential health benefits, including antioxidant and anti-inflammatory properties. This opens up avenues for research into the therapeutic applications of 5-allyl-5-sec-butyl-hexahydropyrimidine-2,4,6-trione.
  • Reaction Dynamics: The presence of multiple functional groups in this compound can lead to a variety of chemical reactions, making it a good candidate for synthetic chemistry studies. Its reactivity can be harnessed for the development of new materials or drug compounds.

"The beauty of organic chemistry lies in the endless possibilities of compound modifications and their resulting properties!"

Research into compounds like 5-allyl-5-sec-butyl-hexahydropyrimidine-2,4,6-trione not only enriches our understanding of organic chemistry but also paves the way for innovative applications in pharmaceuticals, agriculture, and materials science. As scientists continue to explore this intriguing compound, we may uncover novel uses that could have significant impacts on various fields.

Synonyms
TALBUTAL
Lotusate
Profundol
115-44-6
Talbumalum
5-Allyl-5-sec-butylbarbituric acid
Talbutale
Talbutalum
Talbutal [INN]
sec-Butyl allyl barbituric acid
5-Allyl-5-(1-methylpropyl) barbituric acid
WIN 5095
Talbutalum [INN-Latin]
Barbituric acid, 5-allyl-5-sec-butyl-
HSDB 3397
EINECS 204-090-4
UNII-4YIR8202AX
5-(1-Methylpropyl)-5-(2-propenyl)-2,4,6(1H,3H,5H)-pyrimidinetrione
Talbutal (INN)
4YIR8202AX
DTXSID8023630
Talbutal [USP:INN]
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(1-methylpropyl)-5-(2-propenyl)-
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(1-methypropyl)-5-(2-propenyl)-
DTXCID403630
Talbutale [DCIT]
Talbutal (USP:INN)
Talbutalum (INN-Latin)
TALBUTAL (MART.)
TALBUTAL [MART.]
Talbutal (1mg/ml in Acetonitrile)
(RS)-5-allyl-5-sec-butylpyrimidine-2,4,6(1H,3H,5H)-trione
Lotusate (TN)
5-butan-2-yl-5-prop-2-enyl-1,3-diazinane-2,4,6-trione
Latusate
TALBUTAL [HSDB]
TALBUTAL [MI]
TALBUTAL [VANDF]
Talbutal ciii(250 mg)
TALBUTAL [WHO-DD]
SCHEMBL122147
TALBUTAL [ORANGE BOOK]
allyl-sec-butyl-barbituric acid
CHEMBL1200802
N05CA07
CHEBI:134923
Tox21_113715
HY-U00276
5-(1-methylpropyl)-5-prop-2-en-1-ylpyrimidine-2,4,6(1H,3H,5H)-trione
CS-7222
DB00306
NCGC00253567-01
CAS-115-44-6
5-allyl-5-(1-methylpropyl)barbituric acid
NS00023740
D06887
Q409942
5-Allyl-5-sec-butyl-2,4,6(1H,3H,5H)-pyrimidinetrione
5-(1-Methylpropyl)-5-(2-propenyl)-2,4-6(1H,3H,5H)-pyrimidinetrione
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(1-methylpropyl)-5-(2-propen-1-yl)-
204-090-4