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1,3-diphenyl-1,3-butadiene

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Identification
Molecular formula
C16H14
CAS number
538-81-8
IUPAC name
4-phenylbuta-1,3-dienylbenzene
State
State

At room temperature, 1,3-diphenyl-1,3-butadiene is in solid state. It forms distinct crystalline structures which are often off-white or slightly yellow due to the presence of impurities.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.00
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.00
General information
Molecular weight
206.28g/mol
Molar mass
206.2820g/mol
Density
0.9951g/cm3
Appearence

1,3-Diphenyl-1,3-butadiene appears as an off-white or yellow crystalline solid. It may also be encountered in a pale yellow form when impurities are present. The compound is known for its characteristic crystalline structure.

Comment on solubility

Solubility of 4-phenylbuta-1,3-dienylbenzene

When it comes to the solubility of 4-phenylbuta-1,3-dienylbenzene, there are several factors to consider. This compound, a derivative of benzene, exhibits certain characteristics typical of aromatic systems.

  • Polarity: The presence of multiple aromatic rings generally indicates a lower polarity, making the compound more soluble in organic solvents rather than in water.
  • Solvent interactions: 4-phenylbuta-1,3-dienylbenzene shows good solubility in non-polar solvents like hexane and dichloromethane.
  • Temperature dependence: Solubility may increase with temperature, especially in non-polar options, allowing for better dissolution as thermal energy enhances molecular interactions.

For practical applications, understanding its solubility is vital in areas such as organic synthesis and materials science. As a general guideline, when exploring solvents for 4-phenylbuta-1,3-dienylbenzene, one should always prioritize:

  1. Low-polarity solvents for maximum effectiveness.
  2. Temperature adjustments for enhanced solubility.
  3. Avoidance of polar solvents like water, which are less effective.

As a conclusion, while 4-phenylbuta-1,3-dienylbenzene presents challenges in terms of solubility, careful selection of solvent and conditions can facilitate its useful applications in various chemical processes.

Interesting facts

Exploring 4-Phenylbuta-1,3-dienylbenzene

4-Phenylbuta-1,3-dienylbenzene is a fascinating compound, capturing the interest of chemists and students alike. This compound belongs to the class of organic compounds known as aromatic compounds due to its benzene ring structure.

Key Characteristics

  • Structural Diversity: The compound features an extended conjugated system, which consists of a long carbon chain and a phenyl ring. This contributes to its intriguing chemical properties.
  • Optical Properties: The extended π-electron system allows for interesting light absorption characteristics, making it a subject of study in photochemistry.
  • Potential Applications: Compounds like 4-phenylbuta-1,3-dienylbenzene are considered for use in materials science, potentially in organic semiconductors or as intermediates in the synthesis of more complex molecules.
  • Reactivity: The substitution patterns on the aromatic ring can influence the reactivity of this compound, affecting how it participates in various chemical reactions.

Chemical Significance

The study of such compounds assists scientists in understanding conjugation effects and related phenomena in organic chemistry. The fascinating interplay of double bonds within its structure contributes to its unique reactivity and potential applications.

In summary, 4-phenylbuta-1,3-dienylbenzene is not merely a chemical formula; it represents a gateway to exploring fundamental concepts of chemistry, such as aromaticity, reactivity, and the development of new materials. As bookshelves fill with research and discoveries, compounds like this one pave the way for innovations in both organic chemistry and related fields.

Synonyms
886-65-7
Benzene, 1,1'-(1,3-butadiene-1,4-diyl)bis-
1,4-Diphenylbuta-1,3-diene
1,4-Diphenylbutadiene
4-phenylbuta-1,3-dienylbenzene
Distyryl
MFCD00004791
1,4-diphenyl 1,3-butadiene
DTXSID1022132
AKOS028108294
SY112218
DB-057095
NS00042250
Q27122663