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Methyl 4-aminobenzenesulfonylcarbamate

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Identification
Molecular formula
C8H10N2O4S
CAS number
69644-56-4
IUPAC name
methyl N-(4-aminophenyl)sulfonylcarbamate
State
State

This compound is solid at room temperature, typically forming crystalline structures that can be held in powdered or particulate form depending on its specific processing and storage conditions.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
230.25g/mol
Molar mass
230.2510g/mol
Density
1.4115g/cm3
Appearence

Methyl N-(4-aminophenyl)sulfonylcarbamate, also known as Methyl 4-aminobenzenesulfonylcarbamate, appears as a solid compound. It is typically found in a crystalline form and its purity can influence color, with pure samples being white to off-white.

Comment on solubility

Solubility of Methyl N-(4-Aminophenyl)sulfonylcarbamate

Methyl N-(4-aminophenyl)sulfonylcarbamate is known for its unique structure and properties, which can influence its solubility in various solvents. Solubility is an essential characteristic of compounds, impacting their application in fields such as pharmaceuticals, agriculture, and chemical research. Consider the following aspects regarding the solubility of this compound:

  • Polarity: The presence of sulfonyl and carbamate functional groups often increases the polarity of the compound, thus enhancing its interaction with polar solvents such as water.
  • Hydrogen Bonding: Due to the potential for hydrogen bonding through both the amine and carbamate groups, methyl N-(4-aminophenyl)sulfonylcarbamate may exhibit improved solubility in polar organic solvents.
  • Temperature Dependence: It's also noteworthy that the solubility of many organic compounds can vary with temperature; increased temperatures generally lead to enhanced solubility.
  • pH Sensitivity: The solubility could be affected by the pH of the solvent, especially if the compound can exist in different ionic forms under varying pH conditions.

Overall, while detailed solubility data for methyl N-(4-aminophenyl)sulfonylcarbamate may be limited, its structural characteristics suggest a potential for reasonable solubility in both polar and non-polar solvents. Understanding its solubility behavior is crucial for optimizing its use in practical applications.

Interesting facts

Interesting Facts about Methyl N-(4-Aminophenyl)sulfonylcarbamate

Methyl N-(4-aminophenyl)sulfonylcarbamate is a fascinating compound with diverse applications and unique characteristics. Below are some intriguing insights about this compound:

  • Biological Significance: This compound is a key player in medicinal chemistry. Its structure allows it to interact effectively with biological targets, making it a candidate for drug development.
  • Mechanism of Action: Methyl N-(4-aminophenyl)sulfonylcarbamate may act through mechanisms such as inhibition or modulation of specific enzymes, contributing to its therapeutic effects.
  • Sulfonamide Derivative: As a sulfonamide derivative, it inherits properties that can aid in the synthesis of similar compounds, potentially leading to novel therapeutic agents.
  • Research Applications: This compound has drawn interest in the field of organic synthesis. Researchers are exploring its properties for creating more complex chemical entities.
  • Environmental Considerations: Studies on its ecological impact are important, as both sulfonamide compounds and the related sulfonyl groups have been examined for their effects on the environment.

In summary, methyl N-(4-aminophenyl)sulfonylcarbamate not only showcases the elegance of organic synthesis but also holds promise in advancing medicinal research. The ongoing exploration of its properties is a testament to the vibrant and evolving field of chemistry.

"Chemistry is the life blood of every process in the universe," and compounds like methyl N-(4-aminophenyl)sulfonylcarbamate exemplify this truth in their potential to influence health and industry.

Synonyms
ASULAM
3337-71-1
Asulox
Methyl sulfanilylcarbamate
Asulame [ISO-French]
Asulam [ISO]
Asulam [ANSI:BSI:ISO]
Methyl N-(4-aminophenyl)sulfonylcarbamate
N1-Methoxycarbonylsulfanilamide
Methyl 4-aminobenzenesulphonylcarbamate
Asulfox F
AI3-52723
UNII-0Y5ASM7P5S
EINECS 222-077-1
0Y5ASM7P5S
Methyl p-aminobenzenesulfonylcarbamate
EPA Pesticide Chemical Code 106901
BRN 2697523
DTXSID8023890
Methyl N-(4-aminophenylsulfonyl)carbamate
CHEBI:81696
Sulfanilylcarbamic Acid Methyl Ester
ASULAM [MI]
Methyl 4-aminobenzenesulfonylcarbamate
Methyl (4-aminophenylsulfonyl)carbamate
DTXCID603890
HSDB 6556
N(1)-methoxycarbonylsulfanilamide
3-14-00-01967 (Beilstein Handbook Reference)
Asulame (ISO-French)
M & B 9057
Asulam (ANSI:BSI:ISO)
METHYL N-((4-AMINOPHENYL)SULFONYL)CARBAMATE
Carbamic acid, 4-aminobenzenesulfonyl-, methyl ester
N-((4-AMINOPHENYL)SULFONYL)CARBAMIC ACID METHYL ESTER
sodium [(4-aminophenyl)sulfonyl](methoxycarbonyl)azanide
CARBAMIC ACID,((4-AMINOPHENYL)SULFONYL)-, METHYL ESTER
CARBAMIC ACID,[(4-AMINOPHENYL)SULFONYL]-, METHYL ESTER
sodium ((4-aminophenyl)sulfonyl)(methoxycarbonyl)azanide
N-1-Methoxycarbonylsulfanilamide
4Aminobenzolsulfonylmethylcarbamat
Methyl 4aminophenylsulphonylcarbamate
N(sup 1)Methoxycarbonylsulfanilamide
Methyl 4aminobenzenesulphonylcarbamate
Methyl 4aminophenylsulphonyl carbamate
Methyl 4aminobenzenesulphonyl carbamate
Methyl N(4aminobenzenesulfonyl)carbamate
Methyl ((4aminophenyl)sulfonyl)carbamate
Carbamic acid, sulfanilyl, methyl ester (7CI)
Carbamic acid, ((4aminophenyl)sulfonyl), methyl ester
Carbamic acid, sulfanilyl, methyl ester (7CI)(8CI)
222-077-1
689-264-1
vgpyehkoignjkv-uhfffaoysa-n
Asilan
Jonnix
Asulox F
Plakin
Asulox 40
Methyl sulphanilylcarbamate
MB 9057
Carbamic acid, [(4-aminophenyl)sulfonyl]-, methyl ester
Methyl sulfanilyl carbamate
Asulame
M and B 9057
Carbamic acid, sulfanilyl-, methyl ester
Methyl ((4-aminophenyl)sulfonyl)carbamate
Methyl N-(4-aminobenzenesulfonyl)carbamate
Methyl 4-aminobenzenesulphonyl carbamate
4-Amino-benzolsulfonyl-methylcarbamat
Methyl 4-aminophenylsulphonylcarbamate
Methyl 4-aminophenylsulphonyl carbamate
Methyl 4-aminobenzenesulfonyl carbamate
methyl [(4-aminophenyl)sulfonyl]carbamate
Carbamic acid, ((4-aminophenyl)sulfonyl)-, methyl ester
Caswell No. 062A
Asulox F; M and B 9057; MB 9057;Methyl p-aminobenzenesulfonylcarbamate;
Furfenorex (1.0mg/ml in Acetonitrile)
CAS-3337-71-1
N(sup 1)-Methoxycarbonylsulfanilamide
4-Amino-benzolsulfonyl-methylcarbamat [German]
(+)-N-Methyl-N-(1-methyl-2-phenylethyl)-2-furanmethanamine; (+)-N-Methyl-N-(a-methylphenethyl)furfurylamine; Frugalan; d-Furfenorex; d-Furfurylmethylamphetamine;
Methyl sulfanilyl carbamate.
SCHEMBL64856
Carbamic acid, sulfanilyl-, methyl ester (7CI)(8CI)
CHEMBL2137678
methyl 4-aminophenylsulfonylcarbamate
Tox21_201642
Tox21_300851
Asulam 10 microg/mL in Acetonitrile
c1263
MFCD00055534
AKOS015891065
methyl 4-aminophenyl sulphonylcarbamate
KS-5377
CID 6433598
NCGC00160637-01
NCGC00160637-02
NCGC00160637-03
NCGC00160637-04
NCGC00160637-05
NCGC00160637-06
NCGC00254754-01
NCGC00259191-01
AC-12057
Asulam, PESTANAL(R), analytical standard
NS00009629
C18350
Q2868667