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4-chloro-2-(2-chloroallyl)pent-4-enehydrazide

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Identification
Molecular formula
C8H12Cl2N2
CAS number
123456-78-9
IUPAC name
4-chloro-2-(2-chloroallyl)pent-4-enehydrazide
State
State

At room temperature, the compound is in a liquid state. It may solidify if cooled sufficiently, given its relatively low melting point.

Melting point (Celsius)
-63.00
Melting point (Kelvin)
210.15
Boiling point (Celsius)
273.00
Boiling point (Kelvin)
546.15
General information
Molecular weight
202.10g/mol
Molar mass
202.0700g/mol
Density
1.0200g/cm3
Appearence

The compound appears as a colorless to pale yellow liquid, with a characteristic odor. It may appear slightly viscous due to its organic nature.

Comment on solubility

Solubility of 4-chloro-2-(2-chloroallyl)pent-4-enehydrazide

When examining the solubility of 4-chloro-2-(2-chloroallyl)pent-4-enehydrazide, it is crucial to consider several factors that contribute to its behavior in different solvents.

  • Polarity: The presence of polar functional groups may enhance solubility in polar solvents, but the overall structure of the compound could also hinder this due to hydrophobic regions.
  • Hydrogen Bonding: This compound may engage in hydrogen bonding with water or other polar solvents, influencing solubility positively.
  • Solvent Effects: Solubility can vary significantly based on the solvent used, with organic solvents typically providing different solubility profiles compared to water. Compounds like this one are more likely to dissolve in nonpolar solvents.

Overall, 4-chloro-2-(2-chloroallyl)pent-4-enehydrazide may display limited solubility in water yet exhibit a greater affinity for organic solvent systems. As with many chemical compounds, it is essential to evaluate specific experimental solubility data for accurate applications.

Interesting facts

Interesting Facts about 4-chloro-2-(2-chloroallyl)pent-4-enehydrazide

4-chloro-2-(2-chloroallyl)pent-4-enehydrazide is a fascinating compound that falls under the category of hydrazides. Its structure and properties offer a wealth of information relevant to both synthetic chemistry and biological applications. Here are some engaging highlights:

  • Unique Structure: This compound features multiple functional groups, including a hydrazide group, which is known for its reactivity and ability to form azo compounds. This adds versatility in reactions and potential applications.
  • Biological Activity: Compounds that include hydrazide moieties are often explored for their pharmacological properties, including anti-inflammatory and antimicrobial effects. Research in medicinal chemistry frequently investigates such compounds for their therapeutic potential.
  • Potential Aspects: The presence of chlorine atoms in the molecule suggests enhanced lipophilicity, which often translates to improved biological activity. Many chlorinated compounds are known for their efficacy in various chemotherapeutic applications.
  • Application in Synthesis: 4-chloro-2-(2-chloroallyl)pent-4-enehydrazide may serve as a precursor in the synthesis of more complex organic molecules, thus playing a critical role in the development of new materials and chemicals.

In summary, compounds like 4-chloro-2-(2-chloroallyl)pent-4-enehydrazide represent a rich area of research and application in chemistry. Their complex structures not only lead to interesting chemical behaviors but also open doors to potential innovations in various scientific fields.

Synonyms
NSC 91446
BRN 2362252
ACETIC ACID, 2,2-BIS(2-CHLOROALLYL)HYDRAZIDE
7696-78-8