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Allylglycine

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Identification
Molecular formula
C7H9NO3
CAS number
97-39-2
IUPAC name
3-allyl-5-methyl-oxazolidine-2,4-dione
State
State

At room temperature, the compound is a solid. It remains stable in this state under standard conditions.

Melting point (Celsius)
78.00
Melting point (Kelvin)
351.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
157.17g/mol
Molar mass
157.1710g/mol
Density
1.2750g/cm3
Appearence

3-Allyl-5-methyl-oxazolidine-2,4-dione typically appears as a white crystalline solid. The material is characterized by its fine crystalline nature, which can vary in size and form depending on the specific sample and conditions in which it is found.

Comment on solubility

Solubility of 3-allyl-5-methyl-oxazolidine-2,4-dione

The solubility of 3-allyl-5-methyl-oxazolidine-2,4-dione can be considered within the context of its molecular structure and functional groups. As a cyclic compound with both carbonyl and nitrogen functionalities, its interactions with solvents will play a critical role in determining solubility.

  • Polarity: The presence of polar groups, such as carbonyls (C=O), suggests that this compound may exhibit some degree of polarity, potentially allowing for solubility in polar solvents like water.
  • Hydrogen Bonding: The nitrogen in the oxazolidine ring can engage in hydrogen bonding, which may enhance solubility in alcohols and other polar protic solvents.
  • Allyl Group: The allyl substituent might introduce hydrophobic characteristics, consequently affecting solubility in non-polar solvents.
  • Compared Solvents: It may be more soluble in organic solvents such as DMSO (dimethyl sulfoxide) or ethanol than in hexane or other non-polar solvents.

In summary, while specific solubility data may not be readily available, one could infer that 3-allyl-5-methyl-oxazolidine-2,4-dione would likely have variable solubility properties, dependent on the solvent's polarity and ability to engage in hydrogen bonding. Experimentation would be required to confirm the precise solubility characteristics.

Interesting facts

Interesting Facts about 3-allyl-5-methyl-oxazolidine-2,4-dione

3-allyl-5-methyl-oxazolidine-2,4-dione is a fascinating compound belonging to the class of oxazolidines, which are known for their diverse applications in organic synthesis and medicinal chemistry. This compound has garnered interest for several reasons:

  • Cyclic Structure: The oxazolidine ring contributes to the unique reactivity of the compound, allowing it to participate in various chemical reactions such as cycloaddition and nucleophilic substitution.
  • Biological Relevance: Compounds like 3-allyl-5-methyl-oxazolidine-2,4-dione are of interest in drug development due to their potential as intermediates in the synthesis of biologically active molecules. Research is ongoing to explore its effectiveness against certain diseases.
  • Chirality: The presence of substituents in the oxazolidine structure can lead to the formation of chiral centers, which are crucial in the development of enantiomerically pure substances with specified pharmacological activity.
  • Applications in Organic Synthesis: This compound's framework can act as a scaffold for creating complex molecular architectures, making it a valuable building block in synthetic chemistry.

As stated by renowned chemist John D. Roberts, "The design of new chemical entities is often a game of structural understanding and synthesis pathways." The study of 3-allyl-5-methyl-oxazolidine-2,4-dione exemplifies this concept, showcasing how molecular modification can lead to compounds with innovative properties and potential therapeutic applications.

Understanding compounds like 3-allyl-5-methyl-oxazolidine-2,4-dione is vital for chemists aiming to expand the horizons of synthetic methods and improve drug development processes.

Synonyms
Allomethadione
Malazol
Malidone
ALOXIDONE
Allomethadion
526-35-2
Allomethadionum
Alometadiona
3-Allyl-5-methyloxazolidine-2,4-dione
5-methyl-3-prop-2-enyl-1,3-oxazolidine-2,4-dione
BFT641Z2YT
Allydione
2,4-Oxazolidinedione, 5-methyl-3-(2-propenyl)-
Allometadione
Allometadione [DCIT]
Alometadiona [INN-Spanish]
EINECS 208-389-0
Allomethadionum [INN-Latin]
UNII-BFT641Z2YT
BRN 0135052
Allomethadione [INN:BAN:DCF]
5-Methyl-3-(2-propenyl)-2,4-oxazolidinedione
ALOXIDONE [MI]
2,4-Oxazolidinedione, 3-allyl-5-methyl-
ALLOMETHADIONE [INN]
SCHEMBL78301
4-27-00-03214 (Beilstein Handbook Reference)
CHEMBL93070
DTXSID90862119
CHEBI:134781
XWZXRENCCHMZNF-UHFFFAOYSA-N
AKOS006272293
NS00042888
Q27274647
Z1198155422
2,4-OXAZOLIDINEDIONE, 5-METHYL-3-(2-PROPEN-1-YL)-