Interesting facts
Interesting Facts About 2-Chloro-1,3-benzothiazole
2-Chloro-1,3-benzothiazole is a fascinating compound with several intriguing aspects:
- Structural Significance: This compound features a unique fusion of a benzene ring and a thiazole ring, which contributes to its aromatic characteristics and reactivity. The presence of the chlorine atom enhances its electrophilic properties, making it an important intermediate in various chemical reactions.
- Roles in Synthesis: 2-Chloro-1,3-benzothiazole is often employed in the synthesis of pharmaceuticals and agrochemicals. Its derivatives can serve as potent building blocks in the development of new compounds.
- Biological Activity: Research has shown that derivatives of this compound exhibit intriguing biological activities, including antimicrobial, antifungal, and anti-inflammatory properties. These attributes make it a compound of interest in medicinal chemistry.
- Colorimetric Applications: This compound is also recognized for its utility in colorimetric detection methods, especially in environmental chemistry for sensing applications due to its ability to interact with specific analytes.
As highlighted in research studies, the compound has the potential to “bridge the gap” between organic synthesis and applied chemistry. Its versatility showcases how a single molecule can play various roles across multiple scientific disciplines.
In conclusion, 2-chloro-1,3-benzothiazole not only embodies a unique structural feature in the realm of organic compounds but also serves pragmatic purposes in fields ranging from drug discovery to environmental monitoring!
Synonyms
2-Chlorobenzothiazole
615-20-3
2-CHLOROBENZO[D]THIAZOLE
BENZOTHIAZOLE, 2-CHLORO-
USAF EK-2784
UNII-FN1T1Y0P5P
NSC 8442
EINECS 210-415-0
FN1T1Y0P5P
BRN 0116316
DTXSID2052289
AI3-63118
NSC-8442
2-CHLOROBENZO(D)THIAZOLE
DTXCID6030861
EC 210-415-0
4-27-00-01072 (Beilstein Handbook Reference)
210-415-0
bsqlqmlfthjvks-uhfffaoysa-n
inchi=1/c7h4clns/c8-7-9-5-3-1-2-4-6(5)10-7/h1-4
2-Chloro-1,3-benzothiazole
2-Chloro-benzothiazole
2-Benzothiazolyl Chloride
MFCD00005776
Benzothiazole, chloro-
Chlorobenzothiazole
NSC8442
1-Chlorobenzothiazole; 2-Chlorobenzothiazole; 2-Chloro-1,3-benzothiazole; 2-Chlorobenzo[d]thiazole; NSC 8442;
2-chlorobenzthiazole
2-chloro benzothiazole
(2-chloro)benzothiazole
2-chloro-benzo[d]thiazole
2chloro-1,3-benzothiazole
SCHEMBL76778
2-Chlorobenzothiazole, 99%
WLN: T56 BN DSJ CG
2-Chloro-1,3-benzothiazole #
CHEMBL4559874
BCP26714
Tox21_303729
GEO-00655
AKOS000121331
AB00527
CS-W017711
FC31615
FS-1336
NCGC00357038-01
72403-12-4
CAS-615-20-3
DB-028006
C0332
NS00008447
EN300-23023
A15697
D70903
Q27278083
F2144-0001
Z147647040
Solubility of 2-chloro-1,3-benzothiazole
2-chloro-1,3-benzothiazole is an intriguing compound when it comes to its solubility properties. Overall, it exhibits limited solubility in water, which is a characteristic common among many aromatic heterocycles. However, its solubility can vary significantly in organic solvents. Here are a few key points to consider:
In summary, while 2-chloro-1,3-benzothiazole shows limited solubility in water, its preference for organic solvents underscores the importance of solvent polarity and molecular structure in influencing solubility. As the renowned chemist once stated, "Like dissolves like," emphasizing the relationship between solubility and molecular similarity.