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Ethyl N-(4-chlorophenyl)sulfonylcarbamate

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Identification
Molecular formula
C10H12ClNO4S
CAS number
107534-96-3
IUPAC name
ethyl N-(4-chlorophenyl)sulfonylcarbamate
State
State

Ethyl N-(4-chlorophenyl)sulfonylcarbamate is typically a solid at room temperature, presenting as a crystalline powder.

Melting point (Celsius)
115.00
Melting point (Kelvin)
388.15
Boiling point (Celsius)
242.50
Boiling point (Kelvin)
515.65
General information
Molecular weight
289.72g/mol
Molar mass
289.7230g/mol
Density
1.3820g/cm3
Appearence

Ethyl N-(4-chlorophenyl)sulfonylcarbamate is a white to off-white crystalline solid. Its appearance can be described as powdery with a characteristic odor.

Comment on solubility

Solubility of Ethyl N-(4-Chlorophenyl)sulfonylcarbamate

Ethyl N-(4-chlorophenyl)sulfonylcarbamate is a specialized compound whose solubility characteristics can significantly influence its application in various fields, particularly in chemistry and pharmaceuticals. Understanding its solubility is crucial for effective formulation and usage.

Solubility Profile:

  • Solvent Compatibility: This compound shows varying solubility in different solvents. It is generally more soluble in organic solvents, such as ethanol and acetone, due to its organic nature.
  • Water Solubility: Ethyl N-(4-chlorophenyl)sulfonylcarbamate typically has low solubility in water, making it less favorable for aqueous applications.
  • Temperature Dependence: Like many organic compounds, its solubility may increase with elevated temperatures, which can aid in its dissolution.

A deep understanding of the solubility of this compound can assist scientists and researchers in optimizing its usage. As the solubility can be described as influential—often affecting factors such as bioavailability, efficacy, and stability—it is imperative to conduct thorough assessments before application. In laboratory conditions, researchers may find it beneficial to perform solubility tests to determine the optimal conditions for utilizing ethyl N-(4-chlorophenyl)sulfonylcarbamate effectively.

Interesting facts

Interesting Facts about Ethyl N-(4-chlorophenyl)sulfonylcarbamate

Ethyl N-(4-chlorophenyl)sulfonylcarbamate, often referred to as a potent compound in medicinal chemistry, holds significant promise in various fields due to its unique properties.

Key Features

  • Biological Activity: This compound has shown potential as a pharmacological agent, particularly in the development of drugs aimed at treating cancer and other serious diseases.
  • Sulfonamide Group: The inclusion of a sulfonyl group enhances its biological activity and makes it a valuable component in the synthesis of pharmaceuticals.
  • Chlorine Substitution: The presence of the 4-chlorophenyl group can significantly modulate the compound's interaction with biological targets, improving efficacy and selectivity.

Synthesis and Mechanism

The synthesis of ethyl N-(4-chlorophenyl)sulfonylcarbamate typically involves several key steps that integrate various organic reactions. Scientists utilize methods such as:

  1. Nucleophilic substitution reactions for introducing the chlorophenyl group.
  2. Carbamate formation that allows for fine-tuning the pharmacological properties.

Quote: "The subtle alterations in molecular structure can lead to profound differences in biological activity." This quote reflects the importance of understanding chemical modifications in compounds like ethyl N-(4-chlorophenyl)sulfonylcarbamate.

Research Applications

Researchers are actively studying this compound in various scientific areas, including:

  • Drug Discovery: As a model compound for designing new therapeutics.
  • Toxicology: To understand the compound's effects and mechanisms of action at the cellular level.

In summary, ethyl N-(4-chlorophenyl)sulfonylcarbamate is not just a simple chemical entity; it represents a significant opportunity for discovery in the realms of pharmaceuticals and biomedical research.

Synonyms
13945-53-4
ethyl N-(4-chlorophenyl)sulfonylcarbamate
CARBAMIC ACID, N-(p-CHLOROBENZENESULFONYL)-, ETHYL ESTER
BRN 2379919
N-(4-Chlorbenzolsulfonyl)-aethylurethan [German]
N-(4-Chlorbenzolsulfonyl)-aethylurethan
Oprea1_713527
SCHEMBL9128141
DTXSID40161048
ethyl (4-chlorophenyl)sulfonylcarbamate
DA-10779
SR-01000025727
SR-01000025727-1