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Pyrrolo-((3-chlorophenyl)carbamoyloxy)but-2-yne

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Identification
Molecular formula
C15H15ClN2O2
CAS number
282331-70-8
IUPAC name
4-pyrrolidin-1-ylbut-2-ynyl N-(3-chlorophenyl)carbamate
State
State

At room temperature, this compound is in a solid state, characterized by fine, often crystalline, particles or larger crystalline structures.

Melting point (Celsius)
135.00
Melting point (Kelvin)
408.15
Boiling point (Celsius)
375.00
Boiling point (Kelvin)
648.15
General information
Molecular weight
318.80g/mol
Molar mass
318.8000g/mol
Density
1.2000g/cm3
Appearence

The compound typically appears as a white to off-white crystalline solid under normal conditions.

Comment on solubility

Solubility of 4-pyrrolidin-1-ylbut-2-ynyl N-(3-chlorophenyl)carbamate

The solubility of the compound 4-pyrrolidin-1-ylbut-2-ynyl N-(3-chlorophenyl)carbamate in various solvents is an intriguing subject due to its unique structural characteristics. Understanding its solubility can provide insights into its stability and usability in different chemical environments.

Factors Influencing Solubility

  • Polarity: The presence of the polar −NH and −O functional groups can enhance solubility in polar solvents such as water or alcohols.
  • Hydrophobic Interactions: The butynyl group may contribute to hydrophobic interactions, which can decrease solubility in highly polar solvents.
  • Temperature: Like many compounds, its solubility can increase with temperature, which can aid in the dissolution process in various solvents.

Solvent Preference:

  • Polar solvents: Likely to dissolve due to hydrogen bonding and dipole interactions.
  • Non-polar solvents: Possible lower solubility because the compound may experience unfavorable interactions.

In summary, the solubility of 4-pyrrolidin-1-ylbut-2-ynyl N-(3-chlorophenyl)carbamate is influenced by a combination of its functional groups, solvent polarity, and environmental factors. Understanding these aspects is essential for predicting its behavior in various applications.

Interesting facts

Interesting Facts about 4-pyrrolidin-1-ylbut-2-ynyl N-(3-chlorophenyl)carbamate

4-pyrrolidin-1-ylbut-2-ynyl N-(3-chlorophenyl)carbamate is a **specialized compound** that plays a notable role in medicinal chemistry. Here are some engaging insights about this intriguing compound:

  • Pharmacological Potential: This compound belongs to the category of carbamates, which have been extensively studied for their biological activities, including anti-inflammatory and analgesic properties. Researchers delve into its potential therapeutic applications in treating various diseases.
  • Structural Insight: The presence of a pyrrolidine ring makes this compound particularly interesting. Pyrrolidine derivatives are known for their diverse biological activities, enhancing the activity of compounds in leading drug candidates.
  • Chlorinated Aromatics: The 3-chlorophenyl group contributes to the lipophilicity of the compound, which can influence its binding affinity and selectivity at biological targets. This feature is often exploited in the design of pharmaceuticals to achieve desired effects while minimizing side effects.
  • Mechanistic Studies: Scientists are continually investigating the mechanism of action of this compound. Understanding how it interacts at the molecular level with enzymes or receptors can pave the way for new therapeutic strategies.
  • Research Applications: Beyond medicinal applications, this compound can be utilized in *chemical biology* research to explore the effects of specific modifications in drug design, ultimately leading to advancements in pharmacotherapeutics.

As this compound continues to be researched, it holds the promise of contributing to new breakthroughs in the pharmaceutical world, demonstrating the integral relationship between *structure* and *function* in chemical compounds.

Synonyms
15944-43-1
CARBANILIC ACID, m-CHLORO-, 4-(1-PYRROLIDINYL)-2-BUTYNYL ESTER
m-Chlorocarbanilic acid 4-(1-pyrrolidinyl)-2-butynyl ester
4-pyrrolidin-1-ylbut-2-ynyl N-(3-chlorophenyl)carbamate
4-(1-Pyrrolidinyl)-2-butynyl m-chlorocarbanilate
MLS002703951
L8YE647ST7
NSC-107013
NSC 107013
BRN 1386883
NSC107013
UNII-L8YE647ST7
CHEMBL1871440
DTXSID70166662
SMR001570663