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Cyclopent-1-enyl(methyl)phenylcarbamate

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Identification
Molecular formula
C14H17NO2
CAS number
68359-36-2
IUPAC name
cyclopenten-1-yl N-methyl-N-phenyl-carbamate
State
State

At room temperature, cyclopent-1-enyl(methyl)phenylcarbamate is typically in a liquid state. This makes it useful for certain applications in organic synthesis and industrial uses.

Melting point (Celsius)
-9.00
Melting point (Kelvin)
264.15
Boiling point (Celsius)
313.00
Boiling point (Kelvin)
586.15
General information
Molecular weight
229.28g/mol
Molar mass
229.2840g/mol
Density
1.1960g/cm3
Appearence

Cyclopent-1-enyl(methyl)phenylcarbamate appears as a colorless or light-yellow liquid. It is typically clear and may possess a slight odor characteristic of carbamates.

Comment on solubility

Solubility of Cyclopenten-1-yl N-methyl-N-phenyl-carbamate

Cyclopenten-1-yl N-methyl-N-phenyl-carbamate is a fascinating compound with unique solubility characteristics. Understanding solubility is crucial in various applications, from pharmaceuticals to agricultural products.

Key insights about solubility include:

  • Solvent Interaction: The solubility of this compound depends significantly on the polarity of the solvent used. Polar solvents such as water may see limited solubility, while non-polar solvents could dissolve this compound more readily.
  • Temperature Dependence: Like many organic compounds, its solubility can change with temperature. Typically, increasing the temperature enhances solubility in most solvents.
  • Functional Groups: The presence of the carbamate group suggests potential hydrogen bonding, which could influence solubility in polar solvents.

In summary, the solubility of cyclopenten-1-yl N-methyl-N-phenyl-carbamate is influenced by a combination of factors including solvent type, temperature, and its molecular structure. Understanding these elements can help in predicting its behavior and effective usage in different chemical environments.

Interesting facts

Cyclopenten-1-yl N-methyl-N-phenyl-carbamate

Cyclopenten-1-yl N-methyl-N-phenyl-carbamate is a fascinating organic compound known for its unique structural characteristics and potential applications in various fields of chemistry.

Key Features and Properties

  • Structure: This compound features a cyclopentene ring, which contributes to its reactivity and stability in chemical reactions.
  • Functional Groups: The presence of the carbamate functional group provides opportunities for interactions with biological systems, making it relevant in medicinal chemistry.
  • Substituents: The presence of both the N-methyl and N-phenyl groups enhances its lipophilicity, potentially affecting its biological activity.

Potential Applications

The versatility of cyclopenten-1-yl N-methyl-N-phenyl-carbamate may lead to several intriguing applications:

  • Pharmaceutical Development: Compounds with carbamate groups are often investigated for their pharmacological properties and could serve as leads for drug discovery.
  • Agricultural Chemistry: The compound may also find applications in crop protection or as a growth regulator, helping to enhance agricultural productivity.
  • Material Science: Its unique structure allows for potential use in the development of new materials or polymers with specialized properties.

Chemical Reactions

This compound may be involved in various organic reactions, such as:

  • Nucleophilic substitutions: The reactivity of the carbamate can allow for modifications, potentially leading to more complex molecules.
  • Cycloadditions: The cyclopentene moiety can participate in cycloaddition reactions, expanding the diversity of possible derivatives.

In summary, cyclopenten-1-yl N-methyl-N-phenyl-carbamate is an intriguing compound with unique structural features that open the door to various research avenues. Its potential applications in pharmaceuticals, agriculture, and materials science underscore its scientific relevance. As research progresses, this compound may yield exciting discoveries and innovations in organic chemistry.

Synonyms
6132-26-9
Bayer 38800
N-Methylcarbanilic acid 1-cyclopenten-1-yl ester
DTXSID90976806
CARBANILIC ACID, N-METHYL-, 1-CYCLOPENTEN-1-YL ESTER
cyclopent-1-en-1-yl methyl(phenyl)carbamate