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5-Chloro-3-methylbenzoxazol-2-one

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Identification
Molecular formula
C8H6ClNO2
CAS number
56163-51-8
IUPAC name
5-chloro-3-methyl-1,3-benzoxazol-2-one
State
State

Solid at room temperature.

Melting point (Celsius)
94.50
Melting point (Kelvin)
367.65
Boiling point (Celsius)
182.00
Boiling point (Kelvin)
455.15
General information
Molecular weight
181.57g/mol
Molar mass
181.5700g/mol
Density
1.3420g/cm3
Appearence

An off-white to pale yellow crystalline solid.

Comment on solubility

Solubility of 5-chloro-3-methyl-1,3-benzoxazol-2-one

The solubility of 5-chloro-3-methyl-1,3-benzoxazol-2-one can be complex, influenced by several factors that relate to its chemical structure and interactions with solvents.

Key Points on Solubility:

  • Polarities Matter: This compound contains both polar and nonpolar regions, which affects its solubility in various solvents.
  • Common Solvents: It tends to demonstrate solubility in organic solvents such as dimethyl sulfoxide (DMSO) and acetone, while having limited solubility in water.
  • Functional Groups: The presence of the benzoxazole moiety can engage in hydrogen bonding, which enhances solubility in polar solvents to some extent.

"The solubility in a solvent is a balance of solvent/solute interactions versus solute/solute interactions."

To summarize, while 5-chloro-3-methyl-1,3-benzoxazol-2-one exhibits significant solubility in polar organic solvents, its overall behavior in aqueous environments tends to be limited. Understanding these solubility characteristics is crucial for applications in synthesis and formulation processes.

Interesting facts

Interesting Facts about 5-chloro-3-methyl-1,3-benzoxazol-2-one

5-chloro-3-methyl-1,3-benzoxazol-2-one is a fascinating compound with notable chemical properties and potential applications in various fields. Here are some intriguing aspects of this compound:

  • Structural Significance: The unique structure of 5-chloro-3-methyl-1,3-benzoxazol-2-one features a fused benzoxazole ring, which enhances its chemical stability and provides interesting reactivity patterns in organic synthesis.
  • Fluorescence: Compounds in the benzoxazole family often exhibit fluorescence. This characteristic has made them valuable in applications ranging from biological imaging to the development of fluorescent dyes.
  • Pharmacological Potential: Research suggests that benzoxazole derivatives may possess various biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Such capabilities make 5-chloro-3-methyl-1,3-benzoxazol-2-one a candidate for further pharmacological exploration.
  • Role in Material Science: The compound has been investigated for its potential use in the development of high-performance materials, particularly in the area of polymers. Its unique electronic properties can impart desirable traits to polymer matrices.
  • Environmental Applications: Some studies indicate that derivatives like this one may be effective in environmental applications, such as the removal of heavy metals from wastewater due to their ability to form stable complexes.

In summary, 5-chloro-3-methyl-1,3-benzoxazol-2-one serves as an excellent example of how structural diversity in organic compounds can lead to varied and promising applications across scientific disciplines. As research on this compound continues, it may unveil even more exciting possibilities!

Synonyms
5790-90-9
5-Chloro-3-Methylbenzo[d]oxazol-2(3H)-one
5-Chloro-3-methylbenzoxazol-2(3H)-one
2-BENZOXAZOLINONE, 5-CHLORO-3-METHYL-
5-chloro-3-methyl-1,3-benzoxazol-2-one
5-Chloro-3-methyl-2-benzoxazolinone
5-chloro-3-methyl-2,3-dihydro-1,3-benzoxazol-2-one
5-chloro-3-methyl-1,3-benzoxazol-2(3H)-one
NSC 24960
BRN 0140893
NSC24960
SCHEMBL5544722
DTXSID00206621
WLN: T56 BNVOJ B1 HG
3-methyl-5-chloro-2-benzoxazolone
NSC-24960
STK688699
AKOS005601642
DB-263535
CS-0130248
1,3-Benzoxazol-2(3H)-one, 5-chloro-3-methyl-