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2-Benzylideneheptan-1-ol

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Identification
Molecular formula
C14H20O
CAS number
18424-00-9
IUPAC name
2-benzylideneheptan-1-ol
State
State

At room temperature, 2-benzylideneheptan-1-ol is a liquid. It is often used in fragrance applications due to its aromatic properties.

Melting point (Celsius)
21.00
Melting point (Kelvin)
294.15
Boiling point (Celsius)
303.00
Boiling point (Kelvin)
576.15
General information
Molecular weight
204.32g/mol
Molar mass
204.3180g/mol
Density
0.9682g/cm3
Appearence

2-Benzylideneheptan-1-ol is typically observed as a colorless to pale yellow liquid. It has a distinct aromatic odor due to its benzylidene group, similar to floral or fruity scents, making it relatively easy to identify by smell.

Comment on solubility

Solubility of 2-benzylideneheptan-1-ol

The solubility of 2-benzylideneheptan-1-ol, with its unique structure, can display intriguing characteristics. In terms of solubility, consider the following factors:

  • Polarity: The presence of a hydroxyl group (-OH) typically contributes to increased solubility in polar solvents, such as water, due to hydrogen bonding.
  • Hydrophobic Character: The long hydrocarbon chain attached to the benzylidene moiety may impart hydrophobic properties, potentially decreasing solubility in water while enhancing solubility in nonpolar solvents like hexane.
  • Temperature Effects: Similar compounds often exhibit increased solubility at elevated temperatures, making it crucial to consider the effect of temperature on the solubility of 2-benzylideneheptan-1-ol.
  • Complex Formation: This compound could form complexes with certain solutes, particularly when mixed with polar compounds.

In summary, the solubility of 2-benzylideneheptan-1-ol is likely influenced by its molecular characteristics, making it a fascinating subject for study in different solvent systems. As with many organic compounds, the specific solvent choice can lead to varying solubility profiles.

Interesting facts

Interesting Facts about 2-benzylideneheptan-1-ol

2-benzylideneheptan-1-ol, a fascinating compound in the field of organic chemistry, is known for its unique structure and potential applications. Here are some intriguing highlights:

  • Structure and Isomerism: The compound features a benzylidene group attached to a heptan-1-ol backbone, resulting in interesting isomeric forms. Structural diversity is essential in organic synthesis, allowing chemists to explore various reactivity patterns.
  • Potential Applications: Compounds like 2-benzylideneheptan-1-ol are often investigated in medicinal chemistry for their potential anti-inflammatory and analgesic properties. Studying such structures can lead to the development of new pharmaceutical agents.
  • Importance in Synthesis: This compound may serve as a valuable intermediate in organic synthesis. Its functional groups can be modified to yield a variety of derivatives, contributing significantly to synthetic organic chemistry.
  • Natural Occurrence: While not as common in nature, compounds with similar structures can be found in certain plants, where they may play a role in the plant's defense mechanisms or assist in attracting pollinators through their aromas.
  • Research Interest: The study of 2-benzylideneheptan-1-ol and its derivatives may lead to insights into reaction mechanisms, providing a practical learning experience for chemistry students interested in organic synthesis and reaction kinetics.

In conclusion, 2-benzylideneheptan-1-ol represents a valuable compound that fosters exploration and innovation within organic chemistry. Its unique structure, potential uses, and ability to serve as a building block make it a notable subject for both students and researchers alike.

Synonyms
101-85-9
alpha-Amylcinnamyl alcohol
1-Heptanol, 2-(phenylmethylene)-
2-Pentylcinnamic alcohol
2-Pentyl-3-phenylprop-2-en-1-ol
alpha-amyl cinnamyl alcohol
SCHEMBL872839
2-(phenylmethylidene)heptan-1-ol
LIPHCKNQPJXUQF-UHFFFAOYSA-N
AKOS028108453
G92398