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Methyl N-[4-(methoxycarbonylamino)phenyl]sulfonylcarbamate

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Identification
Molecular formula
C11H12N2O6S
CAS number
13763-37-6
IUPAC name
methyl N-[4-(methoxycarbonylamino)phenyl]sulfonylcarbamate
State
State

At room temperature, methyl N-[4-(methoxycarbonylamino)phenyl]sulfonylcarbamate is a solid, and it's commonly found in a crystalline form. This stability at ambient conditions makes it convenient for handling and storage without needing special environmental controls.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.15
General information
Molecular weight
306.30g/mol
Molar mass
306.2990g/mol
Density
1.4100g/cm3
Appearence

This compound is typically observed as a white crystalline solid, indicating a low level of impurities. The crystal structure allows it to be used in various applications where optical clarity or purity is required.

Comment on solubility

Solubility of Methyl N-[4-(Methoxycarbonylamino)phenyl]sulfonylcarbamate

The solubility of methyl N-[4-(methoxycarbonylamino)phenyl]sulfonylcarbamate can be influenced by several factors, including its molecular structure and the nature of the solvent. Here are some key points to consider:

  • Polar Nature: The presence of polar functional groups, such as the sulfonamide and carbamate moieties, suggests that this compound may have reasonable solubility in polar solvents.
  • Solvent Compatibility: Solubility may be enhanced in solvents such as water, methanol, or dimethyl sulfoxide (DMSO), which can effectively stabilize the polar regions of the molecule.
  • pH Dependence: Changes in pH can alter the ionization state of the compound, consequently influencing its solubility. For instance, adjusting the pH may lead to an increase in solubility.
  • Temperature Effects: Generally, increasing the temperature can improve solubility for many compounds. It is advisable to conduct solubility tests at various temperatures.

In summary, while specific solubility data for methyl N-[4-(methoxycarbonylamino)phenyl]sulfonylcarbamate may require experimental determination, its structural characteristics imply a potential for solubility in polar solvents, subject to influences such as solvent type and environmental conditions.

Interesting facts

Interesting Facts about Methyl N-[4-(methoxycarbonylamino)phenyl]sulfonylcarbamate

Methyl N-[4-(methoxycarbonylamino)phenyl]sulfonylcarbamate, a notable compound in the realm of organic chemistry, showcases intriguing characteristics that capture the attention of scientists and students alike. Here are some fascinating aspects of this compound:

  • Functional Versatility: This compound possesses a sulfonyl group, which is known for its ability to enhance the reactivity of adjacent functional groups, making it a valuable building block in synthetic organic chemistry.
  • Role as a Bioactive Molecule: Methyl N-[4-(methoxycarbonylamino)phenyl]sulfonylcarbamate can be explored for potential pharmaceutical applications, especially given its ability to act as a nitrogen-containing motif, resembling structures found in many bioactive compounds.
  • Molecular Modifications: Its structure allows for various modifications to be made. Chemists can tailor the compound for specific reactions, leading to a wide array of derivatives and subsequently broadening its utility in research.
  • Research Applications: Ongoing research often investigates how this compound interacts with biological systems, particularly in medicinal chemistry where it might be evaluated for antimicrobial or anti-cancer activities.
  • Synthetic Techniques: The synthesis of this compound can serve as an excellent educational example in organic chemistry courses, illustrating techniques such as amidation and sulfonylation, crucial processes in the production of complex organic molecules.

In summary, methyl N-[4-(methoxycarbonylamino)phenyl]sulfonylcarbamate invites further exploration within the fields of organic synthesis and medicinal chemistry. It embodies the creativity and complexity chemical scientists strive for in unlocking new therapeutic avenues.

Synonyms
Carbasulam
Acetylasulam
Carbasulam [ISO]
Caswell No. 573I
UNII-37T3H0AML4
37T3H0AML4
EPA Pesticide Chemical Code 573800
DTXSID2041755
M AND B-9555
Carbamic acid, ((4-((methoxycarbonyl)amino)phenyl)sulfonyl)-, methyl ester
METHYL 4-(METHOXYCARBONYLSULFAMOYL)CARBANILATE
METHYL P-METHOXYCARBONYLAMINOBENZENESULFONYLCARBAMATE
CARBANILIC ACID, P-(CARBOXYSULFAMOYL)-, DIMETHYL ESTER
CARBAMIC ACID, (P-PHENYLENESULFONYL)DI-, DIMETHYL ESTER
METHYL (4-(METHOXYCARBONYLAMINO)BENZENE)SULFONYLCARBAMATE
METHYL N-((4-((METHOXYCARBONYL)AMINO)PHENYL)SULFONYL)CARBAMATE
CARBAMIC ACID, N-((4-((METHOXYCARBONYL)AMINO)PHENYL)SULFONYL)-, METHYL ESTER
methyl N-(4-((methoxycarbonyl)amino)benzenesulfonyl)carbamate
methyl N-{4-[(methoxycarbonyl)amino]benzenesulfonyl}carbamate
DTXCID0021755
1773-37-1
methyl N-[4-(methoxycarbonylamino)phenyl]sulfonylcarbamate
SCHEMBL135654
BAA77337
NS00127342
Q27256701