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2,3,3-triphenylprop-2-enenitrile

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Identification
Molecular formula
C22H15N
CAS number
719-13-1
IUPAC name
2,3,3-triphenylprop-2-enenitrile
State
State

2,3,3-Triphenylprop-2-enenitrile is a solid compound at room temperature. It forms well-defined crystals, often utilized in studies involving organic materials.

Melting point (Celsius)
157.00
Melting point (Kelvin)
430.15
Boiling point (Celsius)
548.00
Boiling point (Kelvin)
821.15
General information
Molecular weight
281.37g/mol
Molar mass
281.3500g/mol
Density
1.1574g/cm3
Appearence

2,3,3-Triphenylprop-2-enenitrile is typically a crystalline solid at room temperature. The color of the crystals can range from white to a pale yellow, depending on purity and specific sample conditions. It is often described as having a pleasant aromatic smell due to its phenyl groups.

Comment on solubility

Solubility of 2,3,3-Triphenylprop-2-enenitrile

2,3,3-Triphenylprop-2-enenitrile, known for its complex structure, exhibits interesting solubility characteristics. This compound is primarily organic and consists of multiple phenyl groups attached to a propenenitrile moiety. Here are some key points about its solubility:

  • Solvent Compatibility: It tends to be soluble in organic solvents such as ethanol, acetone, and chloroform, showcasing its non-polar to moderately polar nature.
  • Water Solubility: 2,3,3-Triphenylprop-2-enenitrile is practically insoluble in water due to its hydrophobic phenyl groups, which resist interaction with the polar water molecules.
  • Influence of Temperature: Like many organic compounds, its solubility can increase with temperature, although specific data might vary based on the solvent used and the temperature range.
  • Polarity Considerations: The presence of the nitrile group does provide some polar character, but the overall structure leans towards non-polar interactions, further emphasizing its solubility in organic mediums.

Overall, understanding the solubility of 2,3,3-triphenylprop-2-enenitrile is crucial for applications in organic synthesis and chemical processes. Its limited solubility in water but good performance in organic solvents underscores its role in various chemical environments.

Interesting facts

Discovering 2,3,3-Triphenylprop-2-enenitrile

2,3,3-Triphenylprop-2-enenitrile is a fascinating organic compound that offers a window into the world of aromatic chemistry and synthetic applications. This compound is particularly interesting due to its structure and the versatility it presents in various chemical reactions.

Key Characteristics

  • Aromatic System: The presence of three phenyl groups significantly alters the electronic properties of the compound, making it a potent participant in electrophilic substitution reactions.
  • Versatile Intermediate: It serves as an important intermediate in the synthesis of dyes, pharmaceuticals, and other complex organic compounds.
  • Intriguing Reaction Pathways: This compound can undergo various reactions, including nucleophilic additions, allowing for the formation of diverse functional groups.

Applications in Chemistry

Researchers often explore 2,3,3-triphenylprop-2-enenitrile for its use in developing new materials and understanding fundamental chemical processes. For instance, it can be deployed in:

  • Synthetic Organic Chemistry: Acting as a building block for more complex molecules.
  • Material Science: Potential applications in the formulation of polymers due to its structure’s stability and reactivity.

Scientific Significance

This compound is not just a matter of mere interest; it is frequently studied in academia and industry for its ability to facilitate photochemical reactions. Understanding its properties can lead to innovations in fields such as:

  • Drug Development: Exploring the pharmacological potential of derivatives derived from its structure.
  • Color Chemistry: Contributing to the design of novel dyes and pigments.

In summary, 2,3,3-triphenylprop-2-enenitrile stands out due to its unique structure, significant potential in synthetic chemistry, and applications that resonate across various scientific disciplines. Embracing challenges and exploring the depths of such compounds not only enriches our understanding but also paves the way for future discoveries.

Synonyms
Triphenylacrylonitrile
2,3,3-Triphenylacrylonitrile
6304-33-2
Triphenylcyanoethylene
Acrylonitrile, triphenyl-
2,3,3-triphenylprop-2-enenitrile
2,3,3-Triphenyl-acrylonitrile
ACRYLONITRILE, 2,3,3-TRIPHENYL-
7136-23-4
MLS002608486
CHEBI:34217
Benzeneacetonitrile, alpha-(diphenylmethylene)-
2,3,3-triphenyl-2-propenenitrile
Benzeneacetonitrile, .alpha.-(diphenylmethylene)-
NSC42900
NSC-42900
.alpha.,.beta.-Diphenylcinnamonitrile
Benzeneacetic acid, .alpha.-(diphenylmethylene)-
alpha,beta-Diphenylcinnamonitrile
EINECS 228-610-4
2,3,3-Trifenylakrylonitril [Czech]
NSC 42900
2,3,3-Trifenylakrylonitril
BRN 1980289
alpha-(Diphenylmethylene)benzeneacetic acid
AI3-63069
Benzeneacetic acid, alpha-(diphenylmethylene)-
MFCD00013811
WLN: NCYR&UYR&R
2,3-Triphenylacrylonitrile
33Q5RZG6CP
Acrylonitrile,3,3-triphenyl-
2,3, 3-Triphenylacrylonitrile
CHEMBL305168
SCHEMBL1343904
DTXSID60212329
Acrylonitrile, 2,2,3-triphenyl-
HMS3078C14
.alpha.,.beta.-Triphenylacrylonitrile
AKOS025117037
AS-87645
PD180111
SMR001527234
alpha-(Diphenylmethylene)benzeneacetonitrile
DB-054390
CS-0454461
NS00035267
.alpha.,.beta., .beta.-Triphenylacrylonitrile
G63023
Q27115912