Interesting facts
Interesting Facts about 2-(1,3-benzothiazol-2-yldisulfanyl)-1,3-benzothiazole
The compound 2-(1,3-benzothiazol-2-yldisulfanyl)-1,3-benzothiazole is an intriguing member of the benzothiazole family, known for its extensive applications in medicinal chemistry and materials science.
Key Characteristics
- Dual Functionality: This compound features both benzothiazole and disulfide functionalities, which offer unique properties that can be leveraged in various chemical reactions.
- Biological Relevance: Benzothiazole derivatives have been studied for their potential as pharmacological agents, often exhibiting anti-cancer, anti-inflammatory, and antimicrobial activities.
- Versatile Intermediates: They serve as valuable intermediates in the synthesis of various organic compounds, making them important in pharmaceutical development.
Applications and Uses
This compound's potential doesn't stop at its chemical structure. It is utilized in:
- Drug Design: Researchers are investigating its efficacy in the development of novel therapeutic agents.
- Materials Science: Its unique properties allow for adaptation in the development of advanced materials, such as conductive polymers.
- Environmental Chemistry: Studies have shown that benzothiazole derivatives can play a role in sensing and mitigating environmental pollutants.
Quote to Reflect On
As noted by leading chemists, "The beauty of benzothiazole compounds lies in their versatility, making them a focal point in both synthetic and medicinal chemistry." This belief underscores the significance of 2-(1,3-benzothiazol-2-yldisulfanyl)-1,3-benzothiazole in ongoing research.
In summary, 2-(1,3-benzothiazol-2-yldisulfanyl)-1,3-benzothiazole stands out due to its diverse applications and potential impact on health and technology. Its exploration continues to inspire innovation in scientific research.
Synonyms
120-78-5
2,2'-Dithiobis(benzothiazole)
2,2'-Dithiobisbenzothiazole
Thiofide
Dibenzothiazyl disulfide
Benzothiazyl disulfide
Altax
Benzothiazole disulfide
MBTS
Dibenzothiazolyl disulfide
Benzothiazolyl disulfide
Vulkacit DM
Bis(2-benzothiazyl) disulfide
Pneumax DM
Vulcafor MBTS
Dibenzoylthiazyl disulfide
Bis(benzothiazolyl) disulfide
2,2'-Benzothiazyl disulfide
2-Mercaptobenzothiazole disulfide
Dibenzothiazolyl disulphide
2,2'-DIBENZOTHIAZYL DISULFIDE
Bis(2-benzothiazolyl) disulfide
Ekagom GS
Accel TM
2-Benzothiazolyl disulfide
Vulkacit DM/C
1,2-bis(benzo[d]thiazol-2-yl)disulfane
Royal MBTS
Benzothiazole, 2,2'-dithiobis-
Dibenzthiazyl disulfide
2,2'-Dibenzothiazolyl disulfide
MBTS rubber accelerator
Benzothiazole, dithiobis-
Vulkacit dm/mgc
dibenzothiazol-2-yl disulfide
2-Benzothiazyl disulfide
2,2'-Bis(benzothiazolyl) disulfide
2-Mercaptobenzothiazyl disulfide
2-(1,3-Benzothiazol-2-yldisulfanyl)-1,3-benzothiazole
BTS-SBT
Di-2-benzothiazolyl disulfide
2,2-dithiobis(benzothiazole)
Dithiobis(benzothiazole)
Mercaptobenzthiazyl ether
Naugex MBT
USAF CY-5
2,2'-Dithiobis(1,3-benzothiazole)
USAF EK-5432
CHEBI:53239
Dwusiarczek dwubenzotiazylu
Benzothiazol-2-yl disulfide
di(1,3-benzothiazol-2-yl) disulfide
2,2'-Dithiobis-benzothiazole
2,2'-Dibenzothiazoyl disulfide
2,2'-Dithiobis[benzothiazole]
NSC-2
2,2'-Dithio-bis-benzothiazole
DTXSID1020146
BI-87F4
6OK753033Z
NCGC00091238-02
DTXCID70146
Caswell No. 408A
NSC 2
2,2'-Dibenzothiazyldisulfide
CAS-120-78-5
Benzthiazole disulfide
CCRIS 4637
HSDB 1137
Di(benzothiazol-2-yl) disulphide
Dwusiarczek dwubenzotiazylu [Polish]
EINECS 204-424-9
EPA Pesticide Chemical Code 009202
BRN 0285796
Mercaptobenzothiazole disulfide
AI3-07662
2,2'-Dithio(bis)benzothiazole
Sanceler DM
UNII-6OK753033Z
Perkacit MBTS
MFCD00022874
DBTD
2,2 inverted exclamation marka-Dithiobis(benzothiazole)
dibenzothiazyl disulphide
Dibenzothiazole disulfide
dibenzo thiazyl disulfide
NSC2
Epitope ID:138947
Mercaptobenzothiazolyl ether
2,2'-dithiobisbenzthiazole
EC 204-424-9
Benzothiazole,2'-dithiobis-
Mercaptobenzothiazyl disulfide
SCHEMBL23527
4-27-00-01862 (Beilstein Handbook Reference)
(benzothiazol-2-yl) disulfide
(benzothiazol-2-yl) disulphide
2,2?-Dithiobis(benzothiazole)
CHEMBL508112
di(benzothiazol-2-yl) disulfide
bis(benzothiazol-2-yl)disulphide
bis(benzothiazole-2-yl)disulfide
bis-(benzothiazol-2-yl)disulphide
Di-(benzothiazol-2-yl)-disulfide
Bis(benzothiazole-2-yl) disulfide
bis-(benzothiazol-2-yl) disulfide
bis-(benzothiazol-2-yl) disulphide
Tox21_111106
BDBM50444458
STK171119
AKOS001022311
BIS(2-BENZOTHIAZYL) DISULPHIDE
Tox21_111106_1
2,2'-DIBENZOTHIAZOLE DISULFIDE
2,2'-Dithiobis(benzothiazole), 99%
CS-W009852
DB14201
NSC-677459
1,2-di(benzo[d]thiazol-2-yl)disulfane
DIBENZOTHIAZYL DISULFIDE [VANDF]
NCGC00091238-01
NCGC00091238-03
2,2'-DITHIOBISBENZOTHIAZOLE [MI]
AC-11588
LS-14263
2,2'-disulfanediylbis(1,3-benzothiazole)
WLN: T56 BN DSJ CSS-CT56 BN DSJ
D0538
NS00005023
2,2'-DIBENZOTHIAZYL DISULFIDE [HSDB]
D77699
SBI-0653866.0001
EN300-7399114
SR-01000944767
2-(1,3-benzothiazol-2-yldithio)-1,3-benzothiazole
Q2795423
SR-01000944767-1
Z56754489
F0900-0449
2-(1,3-Benzothiazol-2-yldisulfanyl)-1,3-benzothiazole #
Solubility of 2-(1,3-benzothiazol-2-yldisulfanyl)-1,3-benzothiazole
The solubility characteristics of 2-(1,3-benzothiazol-2-yldisulfanyl)-1,3-benzothiazole can present several intriguing aspects to consider. As a compound containing multiple aromatic and sulfur elements, its solubility may be influenced by factors such as:
In practical applications, understanding the solubility of 2-(1,3-benzothiazol-2-yldisulfanyl)-1,3-benzothiazole is essential. As noted, it is likely to have limited solubility in water due to its aromatic structure but may exhibit better solubility in organic solvents, allowing for its utilization in various chemical processes.
In summary, the solubility of this compound is influenced by multiple factors, and while it may present challenges in aqueous environments, its interaction with organic solvents can provide alternative pathways for effective utilization.