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Identification
Molecular formula
C11H13NO3
CAS number
119-36-8
IUPAC name
isopropyl N-(2-furylmethyl)carbamate
State
State

At room temperature, isopropyl N-(2-furylmethyl)carbamate is found in solid state. It is stable when stored under proper conditions.

Melting point (Celsius)
57.00
Melting point (Kelvin)
330.20
Boiling point (Celsius)
310.50
Boiling point (Kelvin)
583.60
General information
Molecular weight
209.24g/mol
Molar mass
209.2420g/mol
Density
1.1680g/cm3
Appearence

Isopropyl N-(2-furylmethyl)carbamate appears as a crystalline solid. The color can vary but it is typically a white or off-white substance.

Comment on solubility

Solubility of Isopropyl N-(2-furylmethyl)carbamate

The solubility of isopropyl N-(2-furylmethyl)carbamate is a key attribute that can influence its applications in various fields. This compound, known for its unique structure, demonstrates interesting solubility characteristics.

Generally, its solubility can be classified based on the following observations:

  • Polar Solvents: Isopropyl N-(2-furylmethyl)carbamate is expected to be more soluble in polar solvents such as water and alcohols due to the presence of functional groups that can engage in hydrogen bonding.
  • Non-Polar Solvents: Conversely, the compound's solubility in non-polar solvents may be limited, indicating a lower preference for environments devoid of polar interactions.
  • Temperature Effect: Solubility may increase with temperature, a common phenomenon observed in many organic compounds.
  • Concentration: As with many chemical compounds, varying the concentration can lead to differing solubility profiles.

It is essential to note that solubility data can be variable and dependent on numerous factors, including the purity of the compound and specific solvation conditions. For practical applications, conducting solubility tests under the desired conditions will provide the most accurate information.

Interesting facts

Isopropyl N-(2-furylmethyl)carbamate: An Overview

Isopropyl N-(2-furylmethyl)carbamate is an intriguing compound that demonstrates the fascinating interplay between chemistry and nature. Here are some interesting facts that highlight its importance and applications:

  • Pharmacological Potential: This compound possesses properties that may be beneficial in pharmacology. It has been studied for its potential use in areas related to medicinal chemistry, showcasing its versatility.
  • Natural Inspiration: The presence of the furyl group suggests a structural similarity to various natural products, which are often crucial in drug discovery. This connection to nature can inspire further exploration in the field of bioactive compounds.
  • Mechanism of Action: Research has indicated that carbamates play essential roles in biological systems, particularly as enzyme inhibitors. Understanding how isopropyl N-(2-furylmethyl)carbamate interacts at a molecular level can shed light on its potential mechanisms of action.
  • Synthesis Routes: The synthesis of this compound typically involves reactions that illustrate key concepts in organic chemistry. These pathways often highlight the importance of functional group transformations and the subtleties of regioselectivity.
  • Environmental Considerations: Investigating carbamates helps us understand their environmental impact, particularly if they are used as pesticides or herbicides. Evaluating their degradation pathways can guide us in assessing their ecological footprint.
  • Multidisciplinary Studies: This compound illustrates the interdisciplinary nature of modern chemistry, intertwining organic synthesis, medicinal chemistry, and environmental science, inviting collaboration across various fields.

In summary, isopropyl N-(2-furylmethyl)carbamate is not just a chemical entity; it is a bridge to numerous scientific inquiries and advancements. As researchers continue to explore its properties, the insights gained could contribute significantly to medicinal chemistry and environmental sustainability.

Synonyms
5327-28-6
CARBAMIC ACID, FURFURYL-, ISOPROPYL ESTER
NSC 3305
6CL7P9Z0HO
BRN 0151750
NSC-3305
UNII-6CL7P9Z0HO
DTXSID60201394
4-18-00-07083 (Beilstein Handbook Reference)
DTXCID60123885
Isopropyl furfurylcarbamate
propan-2-yl N-(furan-2-ylmethyl)carbamate
WLN: T5OJ BVMVY1&1
NSC3305