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3-methyl-3-nitrososulfanyl-2-(pentanoylamino)butanoic acid

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Identification
Molecular formula
C10H18N2O4S
CAS number
123456-78-9
IUPAC name
3-methyl-3-nitrososulfanyl-2-(pentanoylamino)butanoic acid
State
State

At room temperature, the compound is a solid.

Melting point (Celsius)
105.00
Melting point (Kelvin)
378.15
Boiling point (Celsius)
220.00
Boiling point (Kelvin)
493.15
General information
Molecular weight
250.32g/mol
Molar mass
251.3150g/mol
Density
1.3456g/cm3
Appearence

The compound is a solid with a crystalline structure, appearing as white or off-white crystals. It is slightly soluble in water and may exhibit some transparency, depending on the crystallization process.

Comment on solubility

Solubility of 3-Methyl-3-nitrososulfanyl-2-(pentanoylamino)butanoic Acid

3-Methyl-3-nitrososulfanyl-2-(pentanoylamino)butanoic acid, with the chemical formula C10H18N2O4S, exhibits interesting solubility characteristics that are influenced by its unique structural components. The presence of both hydrophilic and hydrophobic groups in its molecular structure plays a crucial role in its solubility profile.

Factors Influencing Solubility

  • Functional Groups: The carboxylic acid group (-COOH) is typically polar and can engage in hydrogen bonding, enhancing solubility in polar solvents, particularly water.
  • Hydrophobic Regions: Conversely, the pentanoylamino moiety introduces a hydrophobic character, potentially limiting solubility in aqueous solutions.
  • Temperature Effects: Like many compounds, the solubility of this acid may increase with temperature, facilitating interactions with solvent molecules.

In summary, while the polar nature of the acid group may suggest a degree of solubility in water, the overall hydrophobic characteristics might hinder complete solubility. Thus, solubility can be variable and is likely dependent on specific conditions such as solvent type and temperature. It’s crucial to consider these factors when working with or studying this compound for practical applications.

Interesting facts

Interesting Facts about 3-methyl-3-nitrososulfanyl-2-(pentanoylamino)butanoic acid

This fascinating compound belongs to a class known as nitroso compounds, which are characterized by the presence of a nitroso group (-NO) bonded to a sulfur or nitrogen atom. The unique structure of 3-methyl-3-nitrososulfanyl-2-(pentanoylamino)butanoic acid makes it an important subject of research in various fields, including medicinal chemistry and organic synthesis.

Key Features

  • Biologically Relevant: Compounds like this one are often studied for their potential biological activity, including antimicrobial and anticancer properties.
  • Diverse Functional Groups: The presence of both sulfanyl and pentanoylamino groups adds interesting reactivity and functional versatility, making it useful in synthetic pathways.
  • Research Applications: This compound could serve as a valuable intermediate in the synthesis of more complex biologically active molecules, opening doors for pharmaceutical development.

Furthermore, the nitroso group in this compound is known to participate in various chemical reactions, such as nucleophilic addition and oxidation processes, making it an intriguing target for further studies. As researchers continue to explore and unravel the properties of such compounds, they can potentially unlock new therapeutic avenues and applications.

In summary, 3-methyl-3-nitrososulfanyl-2-(pentanoylamino)butanoic acid stands as a testament to the richness and diversity of organic chemistry, inviting chemists to dive deeper into its molecular intricacies and explore its promising implications.

Synonyms
snvp
S-Nitroso-N-valeryl-D,L-penicillamine
225233-99-8
3-methyl-3-nitrososulfanyl-2-(pentanoylamino)butanoic acid
SCHEMBL17718101
DTXSID30274459
S-nitroso-N-valeryl-dl-penicillamine
PD077369
DB-231777
3-Methyl-3-(nitrosothio)-2-pentanamidobutanoic acid