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4-iodobut-2-ynyl N-(4-chlorophenyl)carbamate

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Identification
Molecular formula
C11H9ClINO2
CAS number
65752-47-2
IUPAC name
4-iodobut-2-ynyl N-(4-chlorophenyl)carbamate
State
State

This compound is typically in a solid state at room temperature. It is stable under normal conditions but should be handled with care due to its reactive nature, especially considering the presence of iodine and chlorine in its structure.

Melting point (Celsius)
90.00
Melting point (Kelvin)
363.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
335.56g/mol
Molar mass
335.5640g/mol
Density
1.7200g/cm3
Appearence

4-iodobut-2-ynyl N-(4-chlorophenyl)carbamate is a crystalline solid, characterized by its distinct color which can vary depending on purity. It may appear as a white or off-white powder.

Comment on solubility

Solubility of 4-iodobut-2-ynyl N-(4-chlorophenyl)carbamate

The solubility of 4-iodobut-2-ynyl N-(4-chlorophenyl)carbamate can be characterized by several key factors:

  • Polarity: The presence of both aromatic (4-chlorophenyl) and aliphatic (but-2-ynyl) structures significantly influences the compound's solubility. The overall polarity of the molecule can lead to moderate solubility in polar solvents.
  • Hydrogen Bonding: The carbamate group may engage in hydrogen bonding with polar solvents, which can enhance solubility.
  • Solvent Compatibility: This compound may show better solubility in solvents such as dimethyl sulfoxide (DMSO) or acetone compared to water due to the non-polar nature of the aliphatic segment.
  • Temperature Dependence: Like many organic compounds, solubility may increase with temperature, suggesting that higher temperatures could facilitate greater dissolution.

In summary, the solubility of 4-iodobut-2-ynyl N-(4-chlorophenyl)carbamate is influenced by a combination of its structural features and the nature of the solvent utilized. Experimentation is essential to fully understand its solubility profile in various environments.

Interesting facts

Interesting Facts about 4-Iodobut-2-ynyl N-(4-chlorophenyl)carbamate

4-Iodobut-2-ynyl N-(4-chlorophenyl)carbamate is a fascinating compound that plays an important role in the field of organic chemistry. Here are some intriguing aspects of this chemical:

  • Versatile Intermediates: This compound functions as a versatile intermediate in organic synthesis, particularly in the formation of other complex molecules. Its unique structure allows for various modifications, making it a valuable building block.
  • Biological Activity: Compounds similar to 4-iodobut-2-ynyl N-(4-chlorophenyl)carbamate have been investigated for their biological activities, especially in the development of pharmaceuticals. There may be potential applications in treating various ailments, although more research is necessary.
  • Halogen Chemistry: The presence of iodine introduces interesting reactivity patterns due to its electronegativity. This can facilitate nucleophilic substitution reactions which can be essential in synthesizing target compounds.
  • Applications in Agrochemicals: Carbamates, including this compound, are often evaluated for their effectiveness as pesticides. They can inhibit specific enzymes in pests, leading to their eventual elimination while being less harmful to plants and humans.
  • Research and Development: Ongoing studies are dedicated to discovering new applications and optimizing synthetic routes involving 4-iodobut-2-ynyl N-(4-chlorophenyl)carbamate. This research underscores the dynamic nature of organic compounds in modern chemistry.

The exploration of 4-iodobut-2-ynyl N-(4-chlorophenyl)carbamate highlights the intricate connections between structure and function in chemical compounds. As a chemist or student, delving into its properties opens up numerous avenues for innovative applications and discoveries.

Synonyms
14225-20-8
BRN 3055356
4-Iodo-2-butynyl p-chlorocarbanilate
CARBANILIC ACID, p-CHLORO-, 4-IODO-2-BUTYNYL ESTER
p-Chlorocarbanilic acid 4-iodo-2-butynyl ester
DTXSID00161983
DTXCID6084474
4-iodobut-2-ynyl N-(4-chlorophenyl)carbamate
N-(p-Chlorophenyl)carbamic acid 4-iodo-2-butynyl ester