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Benzylidene malononitrile

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Identification
Molecular formula
C10H6N2
CAS number
622-80-0
IUPAC name
2-(phenylazomethyl)propanedinitrile
State
State

At room temperature, benzylidene malononitrile is in a solid state.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
154.17g/mol
Molar mass
154.1650g/mol
Density
1.0600g/cm3
Appearence

Benzylidene malononitrile appears as a colorless to yellow crystalline solid. It is often used in organic synthesis and can form polymorphic crystal structures depending on the conditions during crystallization.

Comment on solubility

Solubility of 2-(phenylazomethyl)propanedinitrile

The solubility of 2-(phenylazomethyl)propanedinitrile is influenced by several factors that determine how this compound interacts with various solvents.

  • Solvent Polarity: This compound tends to be more soluble in polar organic solvents such as dimethyl sulfoxide (DMSO) or methanol. Its solubility decreases in non-polar solvents.
  • Temperature: An increase in temperature usually enhances solubility. Warm solvents can facilitate the dissolution of solid compounds.
  • Hydrogen Bonding: The presence of functional groups that can engage in hydrogen bonding significantly affects solubility. This compound may form hydrogen bonds with protic solvents.

Overall, understanding the solubility properties of 2-(phenylazomethyl)propanedinitrile is crucial for applications in organic synthesis and formulations.

In summary: The solubility of 2-(phenylazomethyl)propanedinitrile is primarily dictated by polarity, temperature, and hydrogen bonding interactions, making it an interesting subject for further study.

Interesting facts

Interesting Facts about 2-(Phenylazomethyl)propanedinitrile

2-(Phenylazomethyl)propanedinitrile is an intriguing compound that showcases the fascinating intersection of chemistry and molecular design. Here are some noteworthy points about this compound:

  • Structure and Functionality: This compound possesses a unique structure that includes both a nitrile group and an azomethyl functional group, which plays a significant role in its reactivity and interactions with other molecules.
  • Synthetic Applications: The compound can serve as an intermediate in organic synthesis, allowing chemists to create complex molecules for pharmaceuticals and agrochemicals.
  • Biological Activity: Certain derivatives of compounds with similar structures have been reported to exhibit interesting biological properties, making them candidates for further exploration in drug discovery.
  • Research Potential: Its distinctive characteristics invite researchers to delve deeper into its potential uses in various fields such as materials science and biochemistry.

As a chemist, one might find it fascinating to consider the potential mechanisms of action that could arise from derivatives of this compound. For example:

  1. Exploration of antimicrobial properties
  2. Investigation of its effects on enzymatic pathways
  3. Utilization in catalysis for various chemical transformations

In summary, 2-(Phenylazomethyl)propanedinitrile is more than just a chemical entity; it is a portal into a world of scientific discovery and innovation. As we continue to study its properties and reactivity, who knows what exciting developments might arise?

Synonyms
Methyl(phenylazo)malononitrile
3655-89-8
F 2279
Phenyl-azo-methyl-malonitril [German]
Phenyl-azo-methyl-malonitril
BRN 1818999
MALONONITRILE, METHYL(PHENYLAZO)-