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2-nitroso-1-phenyl-prop-1-en-1-ol

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Identification
Molecular formula
C9H9NO2
CAS number
.0000
IUPAC name
2-nitroso-1-phenyl-prop-1-en-1-ol
State
State

At room temperature, 2-nitroso-1-phenyl-prop-1-en-1-ol is generally in a solid state. However, due to its relatively low melting point, it can easily become liquid if the temperature slightly increases.

Melting point (Celsius)
56.00
Melting point (Kelvin)
329.00
Boiling point (Celsius)
205.00
Boiling point (Kelvin)
478.00
General information
Molecular weight
163.19g/mol
Molar mass
163.1870g/mol
Density
1.2300g/cm3
Appearence

2-nitroso-1-phenyl-prop-1-en-1-ol is typically a yellow to orange crystalline solid. It may also exist in a liquid form depending on the temperature and specific conditions.

Comment on solubility

Solubility of 2-nitroso-1-phenyl-prop-1-en-1-ol

The solubility of 2-nitroso-1-phenyl-prop-1-en-1-ol is an intriguing aspect of its chemical properties. This compound, with its structural complexities, exhibits specific behaviors when interacting with solvents. Here are some key points regarding its solubility:

  • Polarity: The presence of the nitroso group and hydroxyl group suggests that the compound may demonstrate significant polarity, which can enhance its solubility in polar solvents such as water.
  • Hydrogen Bonding: The hydroxyl (-OH) group is capable of forming hydrogen bonds, potentially increasing solubility in protic solvents.
  • Organic Solvents: It may also exhibit solubility in organic solvents due to the presence of the phenyl group, which typically increases hydrophobic character.
  • Temperature Dependency: Like many organic compounds, solubility may vary with temperature; higher temperatures often increase solubility in many solvents.

In summary, while the solubility of 2-nitroso-1-phenyl-prop-1-en-1-ol can be influenced by its molecular structure, predicted solubility characteristics suggest significant potential in both polar and non-polar environments. Understanding these nuances can be critical in applications where solubility plays a vital role.

Interesting facts

Interesting Facts about 2-nitroso-1-phenyl-prop-1-en-1-ol

2-nitroso-1-phenyl-prop-1-en-1-ol is a fascinating chemical compound that belongs to a class of organic compounds known for their diverse applications in various fields of science and industry. Here are some noteworthy points about this unique compound:

  • Conditional Reactivity: This compound features a nitroso group, which significantly influences its reactivity and chemical behavior. Nitroso compounds are known to engage in reactions such as nucleophilic addition and electrophilic substitution, showcasing their versatility in organic synthesis.
  • Role in Material Science: Compounds like 2-nitroso-1-phenyl-prop-1-en-1-ol have potential uses in the formulation of polymers and advanced materials. They can act as intermediates or stabilizers in polymerization reactions, leading to the development of new materials with desired properties.
  • Biological Significance: The interactions of nitroso compounds with biological systems have drawn considerable interest. While some nitroso compounds may exhibit toxicity, others serve as important signaling molecules or are involved in nitrogen metabolism.
  • Applications in Synthesis: In synthetic organic chemistry, this compound can be employed in the synthesis of more complex molecules, allowing scientists to create a broad array of natural products and pharmaceuticals.
  • Investigation Tools: The study of nitroso compounds like this one can also shed light on the mechanisms of various chemical reactions, making them valuable for educational purposes and research.

As noted by many chemists, **"Understanding the role of functional groups is pivotal in mastering organic chemistry."** The nitroso group in 2-nitroso-1-phenyl-prop-1-en-1-ol exemplifies how specific structural elements dictate chemical behavior and interactions.

Overall, 2-nitroso-1-phenyl-prop-1-en-1-ol stands out as a notable compound, rich in chemistry and promising in application across several domains, ensuring its relevance in both academic research and industrial efforts.