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2-Phenylbenzothiazole

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Identification
Molecular formula
C13H9NS
CAS number
92-96-6
IUPAC name
2-phenyl-1,3-benzothiazole
State
State

At room temperature, 2-Phenylbenzothiazole is typically in a solid state.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
332.00
Boiling point (Kelvin)
605.15
General information
Molecular weight
211.30g/mol
Molar mass
211.2980g/mol
Density
1.2200g/cm3
Appearence

2-Phenylbenzothiazole is a solid compound with a white to off-white appearance. It generally forms crystalline structures when observed in solid form.

Comment on solubility

Solubility of 2-phenyl-1,3-benzothiazole

2-phenyl-1,3-benzothiazole is a compound that exhibits notable insolubility in water, which is a common characteristic for many organic compounds that possess aromatic structures. This lack of solubility can be attributed to several factors:

  • Hydrophobic Nature: The presence of multiple benzene rings contributes to its hydrophobic nature, making it less likely to interact with polar water molecules.
  • Structural Complexity: The heterocyclic structure containing sulfur and nitrogen can complicate solvation processes, leading to reduced solubility.
  • Low Polarity: With limited polar functional groups to facilitate hydrogen bonding, the overall polarity remains low.

In organic solvents, however, 2-phenyl-1,3-benzothiazole demonstrates significantly better solubility. Common solvents include:

  • Dimethyl sulfoxide (DMSO)
  • Acetone
  • Ethyl acetate

This solubility profile makes it particularly useful for applications in organic synthesis and medicinal chemistry, where its interaction with non-aqueous media is often required.

Interesting facts

Interesting Facts about 2-Phenyl-1,3-benzothiazole

2-Phenyl-1,3-benzothiazole is a fascinating organic compound that belongs to the class of benzothiazoles, which are heterocyclic compounds containing both sulfur and nitrogen in their rings. This compound exhibits intriguing properties and a variety of applications that make it notable in the field of chemistry.

Key Features and Applications

  • Fluorescent Properties: One of the remarkable characteristics of 2-phenyl-1,3-benzothiazole is its ability to exhibit fluorescence. This property makes it useful in the development of fluorescent dyes and labeling agents.
  • Biological Activity: Research has shown that benzothiazole derivatives, including 2-phenyl-1,3-benzothiazole, may possess significant biological activities. For instance, they can act as antibacterial and antifungal agents, contributing to their potential use in medicinal chemistry.
  • Material Science: This compound also finds application in material science. It can be used in the formulation of polymers and other materials, enhancing their properties and performance.
  • Chemical Synthesis: The flexibility of the benzothiazole structure allows chemists to undertake various synthetic transformations, facilitating the creation of new compounds with desirable features.

Research and Discovery

Originally, benzothiazole compounds captured the interest of researchers due to their structural uniqueness and diverse reactivity. The discovery of 2-phenyl-1,3-benzothiazole has opened avenues for exciting research, particularly in:

  1. Organic Synthesis: Investigating new synthetic routes has led to derivatives with tailored properties.
  2. Pharmaceutical Chemistry: The exploration of its bioactivity continues to inspire novel drug candidates.

As you delve into the study of 2-phenyl-1,3-benzothiazole, remember that compounds like this exemplify the intricate relationship between structure and function, inspiring chemists to innovate and explore further. Their potential in various fields emphasizes the importance of continued research in organic chemistry, ultimately benefiting multiple industries.

Synonyms
2-Phenylbenzothiazole
883-93-2
BENZOTHIAZOLE, 2-PHENYL-
NSC 1854
NSC 2034
EINECS 212-935-3
FO573G4BGT
BRN 0141340
AI3-00636
NSC-1854
NSC-2034
DTXSID80236946
4-27-00-01385 (Beilstein Handbook Reference)
Benzothiazole, 2phenyl
2-PBT
DTXCID10159437
212-935-3
2-Phenylbenzo[d]thiazole
2-Phenyl-1,3-benzothiazole
2-phenylbenzthiazole
MFCD00005777
WLN: T56 BN DSJ CR
UNII-FO573G4BGT
2-PHENYL BENZOTHIAZOLE
phenyl-benzothiazole
2-phenylbenzothiazol
SCHEMBL94005
2-Phenylbenzothiazole, 97%
IFLab1_004405
2-Phenyl-1,3-benzothiazole #
CHEMBL2272273
NSC1854
NSC2034
HMS1424I05
AC1645
NSC817068
STK360257
AKOS000454336
AKOS000470728
CCG-103648
NSC-817068
IDI1_010160
NCGC00335906-01
AC-29863
CS-11906
SY032902
DB-057064
CS-0095852
NS00039263
P1130
AB00627448-04
10.14272/XBHOUXSGHYZCNH-UHFFFAOYSA-N.1
SR-01000395348
doi:10.14272/XBHOUXSGHYZCNH-UHFFFAOYSA-N.1
SR-01000395348-1
Q27278099
Z50128948
InChI=1/C13H9NS/c1-2-6-10(7-3-1)13-14-11-8-4-5-9-12(11)15-13/h1-9