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Clopidol

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Identification
Molecular formula
C11H7ClN2
CAS number
2971-90-6
IUPAC name
2-[(4-chlorophenyl)methyl]propanedinitrile
State
State

At room temperature, clopidol is in a solid state as a crystalline powder.

Melting point (Celsius)
252.00
Melting point (Kelvin)
525.15
Boiling point (Celsius)
370.80
Boiling point (Kelvin)
643.95
General information
Molecular weight
220.64g/mol
Molar mass
220.6600g/mol
Density
1.2900g/cm3
Appearence

Clopidol typically appears as a white to off-white crystalline powder. It is odorless and is used in its solid form.

Comment on solubility

Solubility of 2-[(4-chlorophenyl)methyl]propanedinitrile

2-[(4-chlorophenyl)methyl]propanedinitrile, a compound with unique structural characteristics, presents interesting solubility traits in various solvents. Its solubility is primarily influenced by the presence of the propanedinitrile and the 4-chlorophenyl group which can interact differently with solvents based on their polarity.

Solubility Patterns

This compound typically exhibits varying solubility profiles:

  • Polar Solvents: It may show improved solubility in polar solvents such as water, dimethyl sulfoxide (DMSO), or ethanol, largely due to its ability to engage in hydrogen bonding and dipole interactions.
  • Non-Polar Solvents: In contrast, its solubility in non-polar solvents like hexane or toluene may be limited, as the hydrophobic character of the aromatic ring can impede interaction with more polar environments.

Moreover, factors such as temperature and the presence of other solutes can greatly influence its solubility. As a general rule of thumb, the solubility typically increases with temperature.

In conclusion, the solubility of 2-[(4-chlorophenyl)methyl]propanedinitrile demonstrates a complex relationship with solvent type and environmental conditions, which is a key consideration for its applications in chemical processes.

Interesting facts

Interesting Facts About 2-[(4-chlorophenyl)methyl]propanedinitrile

2-[(4-chlorophenyl)methyl]propanedinitrile, also known as a nitrile compound, possesses some intriguing chemical and application properties that make it a topic of interest among chemists. Here are some key highlights:

  • Structure and Reactivity: The compound features a unique molecular structure that includes a propanedinitrile moiety, which exhibits interesting reactivity. Nitriles are known for their ability to undergo hydrolysis to form carboxylic acids, making them valuable intermediates in various synthetic pathways.
  • Pharmacological Potential: Compounds containing chlorophenyl groups often exhibit biological activities. Researchers are exploring the potential of 2-[(4-chlorophenyl)methyl]propanedinitrile in pharmaceutical applications, as modifications to such structures can lead to novel therapeutic agents.
  • Role in Organic Synthesis: This compound can serve as a useful reagent in organic synthesis. Its functional groups allow it to participate in multiple reactions, including nucleophilic addition and substitution processes, enabling the synthesis of more complex molecules.
  • Environmental Considerations: As with many organic compounds, understanding the environmental impact is crucial. Researchers are studying the degradation pathways of nitriles to assess their potential toxicity and persistence in the environment.

As the scientific community continues to investigate the applications and implications of compounds like 2-[(4-chlorophenyl)methyl]propanedinitrile, it is evident that there is much more to discover. As stated in the words of Robert H. Grubbs, a Nobel laureate in Chemistry, "There is no such thing as a compound that has been completely studied." Indeed, every compound opens the door to new questions and discoveries.

Synonyms
MALONONITRILE, (p-CHLOROBENZYL)-
2964-33-2
(p-Chlorobenzyl)malononitrile
BRN 2049775
4-Chlor-benzyl-malonitril [German]
4-Chlor-benzyl-malonitril
Propanedinitrile, ((4-chlorophenyl)methyl)-
(4-chlorobenzyl)malononitrile
4-09-00-03360 (Beilstein Handbook Reference)
SCHEMBL4657515
DTXSID70183819
KZVZSAZGEKLWOJ-UHFFFAOYSA-N
AKOS006279865
2-[(4-chlorophenyl)-methyl]-propanedinitrile