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N-(2-amino-1-methylsulfanyl-2-oxo-ethyl)benzamide

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Identification
Molecular formula
C10H12N2O2S
CAS number
Not available
IUPAC name
N-(2-amino-1-methylsulfanyl-2-oxo-ethyl)benzamide
State
State

At room temperature, N-(2-amino-1-methylsulfanyl-2-oxo-ethyl)benzamide is in a solid state, typically handled as a powder form for chemical processes and storage.

Melting point (Celsius)
117.00
Melting point (Kelvin)
390.15
Boiling point (Celsius)
293.00
Boiling point (Kelvin)
566.15
General information
Molecular weight
226.30g/mol
Molar mass
226.2980g/mol
Density
1.3210g/cm3
Appearence

N-(2-amino-1-methylsulfanyl-2-oxo-ethyl)benzamide appears as an off-white crystalline powder. Its crystalline nature is typical for many organic compounds of this type.

Comment on solubility

Solubility of N-(2-amino-1-methylsulfanyl-2-oxo-ethyl)benzamide

N-(2-amino-1-methylsulfanyl-2-oxo-ethyl)benzamide is a compound that typically exhibits variable solubility depending on the conditions such as temperature and the solvent used. Here are some key points regarding its solubility:

  • Polarity: The presence of amine and sulfonyl groups can enhance solubility in polar solvents like water and ethanol.
  • Hydrogen Bonding: The ability to form hydrogen bonds related to the amine and carbonyl groups may increase interactions with polar solvents, further improving solubility.
  • Solvent Compatibility: While it may dissolve well in polar solvents, it may have limited solubility in non-polar substances due to its relatively polar structure.
  • Temperature Influence: Changes in temperature often affect solubility; generally, solubility increases with temperature in many compounds.

Overall, understanding the solubility behavior of N-(2-amino-1-methylsulfanyl-2-oxo-ethyl)benzamide can provide insights into its applications in various chemical environments.

Interesting facts

Interesting Facts about N-(2-amino-1-methylsulfanyl-2-oxo-ethyl)benzamide

N-(2-amino-1-methylsulfanyl-2-oxo-ethyl)benzamide is an intriguing compound, notable for its unique structure and potential applications in various fields. Here are some fascinating insights:

  • Structural Complexity: The compound features a benzamide backbone with an amino group and a methylsulfanyl substituent, making it a member of the diverse class of sulfur-containing organic molecules. This combination can significantly influence the compound's reactivity and physical properties.
  • Biological Relevance: Compounds like N-(2-amino-1-methylsulfanyl-2-oxo-ethyl)benzamide are of interest in medicinal chemistry, where they may exhibit potential pharmacological activities. Their modification can lead to derivatives with enhanced biological efficacy.
  • Role of Sulfur: The presence of sulfur within the molecular structure often contributes unique characteristics, such as increased catalytic activity or participation in biochemical processes, which are pivotal in drug development.
  • Research Potential: Scientists are continually exploring the synthesis and reactivity of similar synthetic compounds, broadening their use in organic synthesis and expanding their application in various industrial sectors.
  • Versatile Applications: Due to its functional groups, this compound can potentially serve as a building block for more complex molecules, contributing to the design of novel materials and pharmaceuticals.

As we continue to explore the vast landscape of organic chemistry, compounds like N-(2-amino-1-methylsulfanyl-2-oxo-ethyl)benzamide remind us of the intricate relationships between structure, function, and application. Embracing their potential, chemists aim to unlock new possibilities in research and technology.

Synonyms
13452-19-2
BENZAMIDE, N-(CARBAMOYL(METHYLTHIO)METHYL)-
alpha-Methylmercaptohippuramide
BRN 2584485
N-(Carbamoyl(methylthio)methyl)benzamide
NSC177926
NSC 177926
NSC-177926
DS-006504