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ethyl N-(3-morpholinooxadiazol-3-ium-5-yl)carbamate

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Identification
Molecular formula
C9H14N4O4
CAS number
Not available
IUPAC name
ethyl N-(3-morpholinooxadiazol-3-ium-5-yl)carbamate
State
State

At room temperature, ethyl N-(3-morpholinooxadiazol-3-ium-5-yl)carbamate is likely to be a solid, given its organic and ionic nature, although specific data is not available for this compound.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
242.23g/mol
Molar mass
0.0000g/mol
Density
0.0000g/cm3
Appearence

Ethyl N-(3-morpholinooxadiazol-3-ium-5-yl)carbamate's appearance specifics are not widely documented, which is not uncommon for less common or complex compounds. However, compounds of similar structure are often crystalline solids or powders if they are organic salts.

Comment on solubility

Solubility of Ethyl N-(3-morpholinooxadiazol-3-ium-5-yl)carbamate (C9H14N4O4)

Ethyl N-(3-morpholinooxadiazol-3-ium-5-yl)carbamate exhibits notable solubility characteristics that are influenced by its unique chemical structure. Here are some key aspects of its solubility:

  • Water Solubility: This compound is expected to have moderate to high solubility in polar solvents like water due to the presence of both ether and amine functional groups, which can interact favorably with water molecules.
  • Organic Solvents: It is likely soluble in a range of organic solvents such as ethanol or dimethyl sulfoxide (DMSO), owing to the ethyl group enhancing its overall compatibility with non-polar environments.
  • pH Dependence: Its solubility may be influenced by the pH of the solution. The presence of ionizable nitrogen may lead to greater solubility in acidic environments, as protonation can enhance interactions with water.
  • Temperature Effects: As with many compounds, increasing temperature generally increases solubility. Thus, warming the solvent can facilitate the dissolution process for ethyl N-(3-morpholinooxadiazol-3-ium-5-yl)carbamate.

In summary, the compound's solubility behavior can be summarized as:

  • Moderate to High Water Solubility: Favorable for aqueous applications.
  • Good Solubility in Organic Solvents: Versatile for laboratory settings.
  • Influenced by pH: Consideration for diverse experimental conditions.

Understanding the solubility properties of this compound is vital for its applications in research and industry, where the solvent environment plays a crucial role in its effectiveness.

Interesting facts

Interesting Facts about Ethyl N-(3-morpholinooxadiazol-3-ium-5-yl)carbamate

Ethyl N-(3-morpholinooxadiazol-3-ium-5-yl)carbamate is a unique compound with a variety of fascinating aspects that may capture the interest of both chemists and enthusiasts.

Chemical Structure and Functionality

This compound exemplifies the rich diversity of organic chemistry with its complex structure. It includes a morpholino group and an oxadiazole moiety, which are known for:

  • Biological activity: Many compounds containing morpholine derivatives show promising features in medicinal chemistry.
  • Stability: The oxadiazole component contributes to the overall stability of the compound, making it robust under various conditions.

Applications

While not much information is readily available regarding the specific applications of this compound, the following general applications can be considered:

  • Pharmaceutical development: Given its structural components, it could potentially serve as a lead compound in drug development.
  • Pesticide formulations: Carbamates are commonly used in agricultural applications; thus, this compound may have potential use in this area.

Research and Synthesis

The synthesis of this compound provides an interesting challenge for chemists:

  • Utilizing reagents such as isocyanates can be crucial in forming the carbamate functional group effectively.
  • The process of creating the oxadiazole ring involves clever strategies that showcase the beauty of synthetic organic chemistry.

Overall, ethyl N-(3-morpholinooxadiazol-3-ium-5-yl)carbamate stands as a testament to the complexity and potential of chemical compounds, stimulating further research and discovery in various fields of chemistry. It offers a glimpse into the innovative possibilities that arise when different functional groups are combined in novel ways.

Synonyms
molsidomine
Coruno
25717-80-0
188472-37-9
SR-01000003151
N-Ethoxycarbonyl-3-morpholinylsydnone imine
N-Carboxy-3-morpholinosynonimine ethyl ester
KBio3_002188
Spectrum_000276
Prestwick0_000547
Prestwick1_000547
Prestwick2_000547
Spectrum2_001178
Spectrum3_001384
Spectrum4_000808
Spectrum5_001515
Lopac0_000725
BSPBio_002968
KBioGR_001295
KBioSS_000756
DivK1c_000603
SPBio_001195
SPBio_002514
SCHEMBL7804448
SCHEMBL12192334
KBio1_000603
KBio2_000756
KBio2_003324
KBio2_005892
DTXSID60860349
CHEBI:114179
NINDS_000603
IDI1_000603
NCGC00018265-01
SR-01000946621
CU-00000000395-1
SR-01000003151-2
SR-01000003151-4
SR-01000946621-1
BRD-K63861289-001-03-0
BRD-K63861289-001-19-6
Q27195206
Molsidomine, European Pharmacopoeia (EP) Reference Standard
1,2,3-Oxadiazolium, 5-[(ethoxycarbonyl)amino]-3-(4-morpholinyl)-
5-[(ethoxycarbonyl)imino]-3-(morpholin-4-yl)-2H-1,2,3??-oxadiazol-3-ylium