Skip to main content

2,5-Dimethylbenzothiazole

ADVERTISEMENT
Identification
Molecular formula
C9H9NS
CAS number
1204-28-0
IUPAC name
2,5-dimethyl-1,3-benzothiazole
State
State

At room temperature, 2,5-Dimethyl-1,3-benzothiazole is a liquid with high viscosity. It is stable under normal conditions and has a low vapor pressure.

Melting point (Celsius)
15.00
Melting point (Kelvin)
288.15
Boiling point (Celsius)
238.00
Boiling point (Kelvin)
511.15
General information
Molecular weight
149.23g/mol
Molar mass
149.2340g/mol
Density
1.1180g/cm3
Appearence

2,5-Dimethyl-1,3-benzothiazole is typically a clear to light yellow liquid. It can also be found in crystalline form under specific conditions. It has a distinctive aromatic odor.

Comment on solubility

Solubility of 2,5-Dimethyl-1,3-benzothiazole

The solubility of 2,5-dimethyl-1,3-benzothiazole is a fascinating topic, as it exhibits quite specific characteristics that can affect its utility in various applications. This compound is known to be sparingly soluble in water, which can limit its effectiveness in aqueous environments.

Factors Influencing Solubility

Several factors contribute to the solubility of this compound:

  • Polarity: The presence of the benzothiazole ring system and methyl groups impacts its overall polarity.
  • Temperature: As with many compounds, increasing temperature often enhances solubility.
  • Solvent Interaction: The choice of solvent plays a crucial role; 2,5-dimethyl-1,3-benzothiazole may show better solubility in organic solvents like ethanol or acetone than in water.

Overall, while 2,5-dimethyl-1,3-benzothiazole presents challenges in solubility in polar solvents, it can be effectively utilized in non-polar or organic surroundings, making its solubility profile essential for its applications in pharmaceuticals and dyes.

Interesting facts

Interesting Facts about 2,5-Dimethyl-1,3-benzothiazole

2,5-Dimethyl-1,3-benzothiazole is a fascinating compound that belongs to the benzothiazole family, which consists of a heterocyclic organic structure featuring both sulfur and nitrogen. Here are some noteworthy points about this compound:

  • Chemical Structure: The unique structure of 2,5-dimethyl-1,3-benzothiazole allows for various interactions due to the presence of the benzothiazole ring, making it a valuable molecule in organic chemistry.
  • Applications: This compound has found utility in several fields including:
    • Organic Synthesis: It serves as an intermediate in the production of dyes and agricultural chemicals.
    • Pharmaceuticals: The compound has potential applications in the development of new medications due to its biological activity.
  • Biological Activity: 2,5-Dimethyl-1,3-benzothiazole has been studied for its antimicrobial properties, and it may possess antioxidant effects, contributing to its appeal in health-related applications.
  • Toxicology Research: Like many benzothiazole derivatives, research into its toxicity is essential for understanding its safety in various applications. Studies have explored its effects on the environment and human health.
  • Cultural Significance: The benzothiazole group is often referenced in literature and scientific discussions, emphasizing its importance in both educational and practical contexts.

The compound's ability to engage with both students and seasoned scientists lies in its versatility and the opportunities it presents for further research. As a testament to chemical innovation, 2,5-dimethyl-1,3-benzothiazole invites ongoing exploration into its myriad applications and effects.

Synonyms
2,5-Dimethylbenzothiazole
95-26-1
2,5-Dimethyl-1,3-benzothiazole
BENZOTHIAZOLE, 2,5-DIMETHYL-
2,5-Dimethylbenzo[d]thiazole
2,5-Dimethylbenzthiazol
BRN 0116455
2,5-Dimethylbenzthiazol [Czech]
F8YB2EH8TU
EINECS 202-404-4
MFCD00005796
DTXSID9059121
4-27-00-01101 (Beilstein Handbook Reference)
2,5-dimethylbenzothiazol
UNII-F8YB2EH8TU
SCHEMBL92781
DTXCID2048951
CHEBI:194732
2,5-Dimethyl-1,3-benzothiazole #
STK396270
AKOS000121363
AS-58494
SY048541
CS-0063216
D1218
NS00040441
D73290
Z56347238
InChI=1/C9H9NS/c1-6-3-4-9-8(5-6)10-7(2)11-9/h3-5H,1-2H
202-404-4