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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
4-pyrrolidin-1-ylbut-2-ynyl N-methylcarbamate
State
State

Carbaryl is typically found as a solid at room temperature.

Melting point (Celsius)
142.50
Melting point (Kelvin)
415.65
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2330g/cm3
Appearence

Carbaryl is a white crystalline solid. It is odorless or may have a faint odor.

Comment on solubility

Solubility of 4-pyrrolidin-1-ylbut-2-ynyl N-methylcarbamate

The solubility of 4-pyrrolidin-1-ylbut-2-ynyl N-methylcarbamate is a critical consideration, especially in pharmaceutical applications. This compound features both polar and nonpolar characteristics, influencing its solubility profile.

Key Factors Affecting Solubility:

  • Polarity: The presence of the N-methylcarbamate group enhances the compound's polar interactions, promoting solubility in polar solvents such as water.
  • Functional Groups: The configuration of the pyrrolidine ring and the alkyne moiety may affect interactions with solvent molecules, contributing to both hydrophilic and lipophilic properties.
  • Temperature: Generally, an increase in temperature can enhance solubility for many organic compounds, including this carbamate derivative.

In practical applications, it's essential to conduct solubility tests under various conditions to gain insights into the effective use of 4-pyrrolidin-1-ylbut-2-ynyl N-methylcarbamate. Such evaluations help in determining its feasibility for formulations and therapeutic delivery mechanisms.

As highlighted in many studies, the solubility of this compound can exhibit variability based on environmental factors and interactions with other substances, which remains a point of interest for further research.

Interesting facts

Interesting Facts about 4-pyrrolidin-1-ylbut-2-ynyl N-methylcarbamate

4-pyrrolidin-1-ylbut-2-ynyl N-methylcarbamate is a chemical compound that belongs to the class of carbamates, which are widely recognized for their diverse applications in both medicinal chemistry and agricultural chemistry. Here are some intriguing aspects of this compound:

  • Innovative Applications: This compound has been studied for its potential in the field of organic synthesis and pharmaceuticals. It is of interest due to its unique structure that combines a pyrrolidine ring with a propargyl group.
  • Mechanism of Action: Compounds like this often act as enzyme inhibitors, and this specific structure could offer insights into how to design more effective therapeutic agents targeting various biological pathways.
  • Carbamate Features: The N-methylcarbamate moiety is significant, as carbamates are known to provide a balance of reactivity and stability, making them suitable for various chemical transformations.
  • Research Opportunities: The compound's unique structure provides excellent opportunities for exploration in medicinal chemistry, particularly in the search for new pharmacophores for drug development.

As noted by chemists, "The beauty of chemistry lies not only in the compounds themselves but in the stories they tell about molecular interactions and potential innovations."

This compound is a prime example of how chemical structures can inspire research across multiple disciplines, highlighting the importance of understanding and exploring chemical diversity. Its intriguing properties warrant further investigation to unlock its full potential in various scientific fields.

Synonyms
16253-32-0
BRN 1370819
CARBAMIC ACID, METHYL-, 4-(1-PYRROLIDINYL)-2-BUTYNYL ESTER
Methylcarbamic acid 4-(1-pyrrolidinyl)-2-butynyl ester
DTXSID20167386
DTXCID3089877
4-pyrrolidin-1-ylbut-2-ynyl N-methylcarbamate