Interesting facts
Interesting Facts about 1,3-Benzothiazol-2-yl N,N-Diethylcarbamodithioate
1,3-Benzothiazol-2-yl N,N-diethylcarbamodithioate, often referred to as a benzothiazole derivative, is a compound that has garnered interest in various fields due to its unique properties and potential applications. Here are some fascinating aspects to consider:
- Structure and Stability: The compound features a benzothiazole ring, which is known for its structural stability and ability to participate in a range of chemical reactions. This is primarily due to the presence of nitrogen and sulfur in the ring system, contributing to the compound's reactivity.
- Biological Activity: Benzothiazole derivatives are often studied for their biological properties. Many compounds in this class have exhibited promising antifungal, antibacterial, and anticancer activities, making them interesting targets for drug discovery.
- Applications in Agriculture: The diethylcarbamodithioate portion of the molecule suggests potential uses in agrochemicals. Some derivatives have been explored for their efficacy as pesticides or fungicides, offering solutions for crop protection.
- Photophysical Properties: The electronic characteristics of benzothiazole compounds often result in interesting photophysical behaviors. They may display fluorescence or phosphorescence, making them suitable for applications in optoelectronic devices and sensors.
- Research Potential: Ongoing research is actively exploring how slight modifications to the chemical structure of benzothiazole can lead to new compounds with enhanced properties. Scientists are particularly interested in the balance between stability and reactivity in such derivatives.
As you delve into the world of 1,3-benzothiazol-2-yl N,N-diethylcarbamodithioate, keep in mind that this is just the tip of the iceberg! The versatility and complexity of benzothiazole derivatives continue to inspire numerous scientific inquiries, making them a subject of great interest in the chemical sciences.
Synonyms
95-30-7
2-Benzothiazolyl diethyldithiocarbamate
Ethylac
Diethyldithiocarbamic acid 2-benzothiazolyl ester
Carbamodithioic acid, diethyl-, 2-benzothiazolyl ester
Benzothiazol-2-yl diethyldithiocarbamate
NSC 4035
2-Benzothiazyl-N,N-diethylthiocarbamylsulfide
2-Benzothiazyl N,N-diethylthiocarbamoyl sulfide
N,N-Diethylthiocarbamoyl 2-benzothiazolyl sulfide
1,3-benzothiazol-2-yl N,N-diethylcarbamodithioate
2-(N,N-Diethyldithiocarbamyl)benzoathinzole
Benzo[d]thiazol-2-yl diethylcarbamodithioate
EINECS 202-408-6
2-((N,N-Diethyldithio)carbamyl)benzoathiazole
BRN 0220149
N,N-Diethylthiocarbamyl-2-benzothiazolyl sulphide
Diethyldithiocarbamic acid, 2-benzothiazolyl ester
ACCELERATOR E
2-Benzothiazolethiol, diethyldithiocarbamate (ester)
NSC-4035
Carbamodithioic acid, N,N-diethyl-, 2-benzothiazolyl ester
NOCCELER-64
2-Benzothiazolyl-N,N-diethylthiocarbamyl sulfide
1-(1,3-benzothiazol-2-ylsulfanyl)-N,N-diethylmethanethioamide
19V77729YZ
CARBAMIC ACID, DIETHYLDITHIO-, 2-BENZOTHIAZOLYL ESTER
N,N-Diethylthiocarbamoyl-2-benzothiazolyl sulfide
2-Benzothiazolyl-N,N-(diethylthio)carbamyl sulfide
2-Benzothiazolethiol, (diethyldithio)carbamate (ester)
2-[(N,N-Diethyldithio)carbamyl]benzoathiazole
UNII-19V77729YZ
MFCD00059887
SCHEMBL78509
DTXSID4059122
LFMQNMXVVXHZCC-UHFFFAOYSA-
NSC4035
AKOS015898528
WLN: T56 BN DSJ CSYUS&N2&2
AS-69599
2-Benzothiazolethiol, diethyldithiocarbamate
1,3-Benzothiazol-2-yl diethyldithiocarbamate
2-(n,n-diethylthiocarbamoylthio)benzothiazole
CS-0205216
D0248
NS00040444
1,3-Benzothiazol-2-yl diethyldithiocarbamate #
E79437
Q27252132
1-benzothiazol-2-ylsulfanyl-N,N-diethyl-methanethioamide
InChI=1/C12H14N2S3/c1-3-14(4-2)12(15)17-11-13-9-7-5-6-8-10(9)16-11/h5-8H,3-4H2,1-2H3
Solubility of 1,3-benzothiazol-2-yl N,N-diethylcarbamodithioate
The solubility of 1,3-benzothiazol-2-yl N,N-diethylcarbamodithioate can be quite interesting due to its unique molecular structure. This compound is a derivative of benzothiazole, which typically affects solubility due to the presence of heteroatoms and functional groups. Here are some key points to consider:
In conclusion, the solubility of 1,3-benzothiazol-2-yl N,N-diethylcarbamodithioate is dictated by its molecular interactions and the surrounding solvent systems. Understanding these properties is essential for applications in pharmaceuticals and agrochemicals.