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Ethyl N-(3-nitrophenyl)sulfonylcarbamate

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Identification
Molecular formula
C10H11N3O6S
CAS number
776308-72-0
IUPAC name
ethyl N-(3-nitrophenyl)sulfonylcarbamate
State
State

At room temperature, ethyl N-(3-nitrophenyl)sulfonylcarbamate is present in a solid state. It is relatively stable under standard laboratory conditions.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.15
Boiling point (Celsius)
355.00
Boiling point (Kelvin)
628.15
General information
Molecular weight
292.27g/mol
Molar mass
292.2690g/mol
Density
1.3900g/cm3
Appearence

Ethyl N-(3-nitrophenyl)sulfonylcarbamate appears as a pale yellow solid. It is typically crystalline in nature which can vary slightly in hue based on its purity and the specific conditions under which it is observed.

Comment on solubility

Solubility of Ethyl N-(3-nitrophenyl)sulfonylcarbamate

Ethyl N-(3-nitrophenyl)sulfonylcarbamate is a compound that exhibits unique solubility characteristics influenced by its molecular structure. The solubility of this compound can be contextualized in several key aspects:

  • Polarity: The presence of the sulfonyl group and the nitro group contributes to a higher polarity, which impacts its ability to dissolve in various solvents.
  • Solvent Compatibility: This compound is likely to be more soluble in polar solvents such as dimethyl sulfoxide (DMSO) or water due to its polar functional groups.
  • Temperature Effects: Like many organic compounds, its solubility may increase with temperature, making it essential to consider temperature when conducting experiments or applications.
  • pH Influence: The solubility can also be altered by the pH of the solution. The ionization of the carbamate group under certain pH conditions can enhance solubility in aqueous solutions.

In summary, the solubility of ethyl N-(3-nitrophenyl)sulfonylcarbamate is defined by a complex interplay of its chemical structure and the solvent's properties. Understanding these factors can significantly aid in optimizing its use in various chemical applications.

Interesting facts

Interesting Facts About Ethyl N-(3-nitrophenyl)sulfonylcarbamate

Ethyl N-(3-nitrophenyl)sulfonylcarbamate is a fascinating compound that combines elements of organic chemistry and pharmacology. Here are some intriguing aspects of this compound:

  • Unique Structure: This compound features a sulfonyl group attached to a nitrophenyl moiety, which is known for its ability to influence the compound's reactivity and biological activity.
  • Biological Significance: Compounds like ethyl N-(3-nitrophenyl)sulfonylcarbamate are often investigated for their potential medicinal properties, particularly in drug development. They may exhibit biological activities that can be harnessed for therapeutic purposes.
  • Applications in Synthesis: The sulfonyl moiety serves as an essential functional group in organic synthesis, allowing for the formation of various derivatives. This makes it a valuable tool in medicinal chemistry.
  • Environmental Impact: Due to the presence of the nitro group, ethyl N-(3-nitrophenyl)sulfonylcarbamate can undergo transformations in the environment, raising questions about its stability and degradation pathways.
  • Research Opportunities: Ongoing studies on this compound can contribute to a better understanding of its mechanism of action and potential applications in fields such as agrochemicals and pharmaceuticals.

In conclusion, ethyl N-(3-nitrophenyl)sulfonylcarbamate stands out as a compound of interest due to its complex structure and potential applications in science. Its study offers a glimpse into the intricate world of chemical interactions and the exciting discoveries that await in the realm of chemical research!

Synonyms
22819-24-5
CARBAMIC ACID, ((m-NITROPHENYL)SULFONYL)-, ETHYL ESTER
BRN 2667086
Ethyl N-(m-nitrophenylsulfonyl)carbamate
Benzenesulfonamide, N-(ethoxycarbonyl)-m-nitro-
DTXSID70177374
4-11-00-00184 (Beilstein Handbook Reference)
RefChem:331716
DTXCID0099865
ethyl N-(3-nitrophenyl)sulfonylcarbamate
Ethyl ((3-nitrophenyl)sulfonyl)carbamate
ETHYL N-(3-NITROBENZENESULFONYL)CARBAMATE
SCHEMBL1969168
AKOS001322170
ethyl (3-nitrophenyl)sulfonylcarbamate
DA-07903
CS-0348211
EN300-43745
SR-01000424032
SR-01000424032-1