Skip to main content

2-Benzylbenzoxazole

ADVERTISEMENT
Identification
Molecular formula
C14H11NO
CAS number
1563-38-8
IUPAC name
2-benzyl-1,3-benzoxazole
State
State

At room temperature, 2-Benzylbenzoxazole is generally in a solid state.

Melting point (Celsius)
72.00
Melting point (Kelvin)
345.00
Boiling point (Celsius)
344.00
Boiling point (Kelvin)
617.00
General information
Molecular weight
211.26g/mol
Molar mass
211.2560g/mol
Density
1.1827g/cm3
Appearence

2-Benzylbenzoxazole is a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-benzyl-1,3-benzoxazole

2-benzyl-1,3-benzoxazole exhibits solubility characteristics that can be intriguing for chemists and researchers. Understanding its solubility in various solvents can aid in practical applications and processing. Here are key points to consider:

  • Solvent Polarity: The solubility of 2-benzyl-1,3-benzoxazole is influenced by the polarity of the solvent used. Generally, it tends to be more soluble in polar aprotic solvents such as dimethyl sulfoxide (DMSO) and acetone.
  • Insolubility in Water: This compound is typically insoluble in water due to its nonpolar aromatic structure, which does not favor interactions with polar water molecules.
  • Common Solvents: In organic chemistry, 2-benzyl-1,3-benzoxazole can show appreciable solubility in common organic solvents including:
    1. Toluene
    2. Chloroform
    3. Ethyl acetate
  • Practical Implications: Its solubility profile indicates that 2-benzyl-1,3-benzoxazole may be effectively utilized in synthetic reactions and extraction processes where non-aqueous environments are favorable.

In summary, while 2-benzyl-1,3-benzoxazole may pose challenges for solubility in aqueous solutions, it demonstrates versatile solubility in a range of organic solvents, making it a valuable compound for various chemical applications.

Interesting facts

Interesting Facts about 2-benzyl-1,3-benzoxazole

2-benzyl-1,3-benzoxazole is a fascinating compound that combines an aromatic ring structure with a heterocyclic component, making it noteworthy in various fields of research. Here are some compelling aspects of this compound:

  • Heterocyclic Chemistry: As a heterocyclic compound, 2-benzyl-1,3-benzoxazole features nitrogen and oxygen atoms in its ring, which can influence electronic properties and reactivity.
  • Pharmacological Potential: Compounds like 2-benzyl-1,3-benzoxazole are of interest in medicinal chemistry as they may exhibit biological activities, including antimicrobial and antioxidant properties.
  • Fluorescent Properties: Some derivatives related to benzoxazole compounds are known for their luminescent properties, making them useful in applications like fluorescent probes and sensors.
  • Material Science: The unique structural characteristics of this compound lend it potential applications in developing novel materials, including polymers and dyes.

Overall, 2-benzyl-1,3-benzoxazole is just one of many fascinating compounds that showcase the interplay between organic synthesis, drug discovery, and material science. Its diverse potential applications continue to inspire researchers across different fields. As noted by chemists, "The beauty of chemistry lies in the endless possibilities that each molecule presents."


Continued research on such compounds not only advances our understanding of chemical properties but also leads to innovative solutions in science and technology.

Synonyms
Benzoxazole, 2-(phenylmethyl)-
2-Benzylbenzoxazole
2-Benzyl-1,3-benzoxazole
BENZOXAZOLE, 2-BENZYL-
2-Benzyl benzoxazole
2008-07-3
MLS000532181
SMR000137122
EINECS 217-914-2
BRN 0159498
2-benzylbenzo[d]oxazole
2-(Phenylmethyl)benzoxazole
Cambridge id 5190862
B95Q4F7AJY
CBDivE_015746
cid_16179
2-Benzyl-1,3-benzoxazole #
CHEMBL233703
SCHEMBL4650036
BDBM62983
DTXSID50173899
HMS1577J16
HMS2471O07
2-(phenylmethyl)-1,3-benzoxazole
NCGC00245724-01
NS00045021
AB00075078-01
4-27-00-01395 (Beilstein Handbook Reference)
SR-01000198118
SR-01000198118-1
Z2049693686
InChI=1/C14H11NO/c1-2-6-11(7-3-1)10-14-15-12-8-4-5-9-13(12)16-14/h1-9H,10H