Interesting facts
Interesting Facts about N-(1,3-benzothiazol-2-ylsulfanyl)-2-methyl-propan-2-amine
N-(1,3-benzothiazol-2-ylsulfanyl)-2-methyl-propan-2-amine, also known as a benzothiazole derivative, showcases some intriguing properties and potential applications in various fields. Here are some noteworthy facts:
- Chemical Relevance: This compound incorporates a benzothiazole moiety, which is known for its versatility in organic synthesis and material chemistry. Benzothiazole derivatives are often used in the development of fluorescent materials and antimicrobial agents.
- Biological Activity: Compounds containing the benzothiazole structure often exhibit significant biological activities. Studies have shown that they can have effects as antitumor, antiviral, and anti-inflammatory agents, drawing interest for potential pharmaceutical applications.
- Stability and Reactivity: The sulfanyl (-S-) group in this compound enhances its reactivity and can participate in various chemical reactions, making it an engaging subject of study for synthetic chemists.
- Environmental Role: Benzothiazole derivatives are also studied for their environmental impact, particularly in assessing their potential as pollutants or in understanding their environmental degradation pathways.
In the words of famous chemist Marie Curie, "Nothing in life is to be feared, it is only to be understood." Researching compounds like N-(1,3-benzothiazol-2-ylsulfanyl)-2-methyl-propan-2-amine fosters understanding and encourages innovation. As scientists delve deeper into this compound, the possibilities it holds for future applications are truly exciting!
Synonyms
N-tert-Butyl-2-benzothiazolesulfenamide
95-31-8
Santocure NS
Nocceler NS
Vulkacit NZ
Accel BNS
Pennac Tbbs
2-(TERT-BUTYLAMINOTHIO)BENZOTHIAZOLE
Vanax NS
S-(Benzo[d]thiazol-2-yl)-N-(tert-butyl)thiohydroxylamine
2-Benzothiazolesulfenamide, N-(1,1-dimethylethyl)-
2-Benzothiazolesulfenamide, N-tert-butyl-
Benzothiazolyl-2-tert-butylsulfenamide
N-tert-Butyl-2-benzothiazylsulfenamide
N-tert-Butylbenzothiazole-2-sulphenamide
NSC 84176
Santocure NS vulcanization accelerator
N-t-Butylbenzothiazylsulfenamide
HSDB 5288
N-tert-Butyl-2-benzothiazolyl sulfenamide
EINECS 202-409-1
N-t-Butyl-2-benzothiazolesulfenamide
N-(1,3-benzothiazol-2-ylsulfanyl)-2-methylpropan-2-amine
BRN 0158370
W468IFJ99C
DTXSID7026572
SULFENAMIDE TBBS
N-(1,1-Dimethylethyl)benzothiazolesulfenamide
NSC-84176
Benzothiazolesulfenamide, N-(1,1-dimethylethyl)-
RHENOGRAN TBBS 80
DTXCID506572
EC 202-409-1
2-[(tert-Butylamino)sulfanyl]-1,3-benzothiazole
n-tert-butyl-2-benzothiazole sulfenamide
2-(TERT-BUTYLAMINOTHIO)BENZOTHIAZOLE [HSDB]
BUTYL-2-BENZOTHIAZOLE SULFENAMIDE, N-TERT-
NS-P; NSC 84176; NSG; Nocceler NS-P; Perkacit TBBS
S-(Benzo[d]thiazol-2-yl)-N-(tert-butyl)-thiohydroxylamine
Accelerator BBTS
Akrochem BBTS
NTBBTS
TBBS
C11H14N2S2
UNII-W468IFJ99C
Santocure TBBS
Perkacit TBBS
Delac NS
Vanax TBSI
Vulkacit NZ/EG
MFCD00022873
N-tert-Butyl-2-benzothiazosulfenamide
BBTS
NtButylbenzothiazylsulfenamide
SCHEMBL80374
NtButyl2benzothiazolesulfenamide
CHEMBL3182037
NtertButyl2benzothiazylsulfenamide
Butyl 2-benzothiazole sulfenamide
Benzothiazolyl2tertbutylsulfenamide
NtertButyl2benzothiazolesulfenamide
HMS1675L02
NSC84176
NtertButyl2benzothiazolyl sulfenamide
Tox21_200895
2Benzothiazolesulfenamide, Ntertbutyl
MSK001865
STK771202
n-t-butyl-2-benzothiazole sulfenamide
AKOS000520589
N-t-Butyl-2-benzothiazole-sulfenamide
N-tert-Butyl-2-benzothiazolesulfenamid
FB33606
N-t-Butyl-2-benzothioazole sulfenamide
CAS-95-31-8
N-t-Butyl-O-benzothiazole-2-sulfenamide
N-tert-Butyl-2-benzothiazolesulphenamide
N-tert-Butyl-2-benzothiazolylsulfenamide
NCGC00248869-01
NCGC00258449-01
WLN: T56 BN DSJ CSMX1&1&1
AS-15571
N-tert-butyl-2-(4-piperidyloxy)acetamide
1ST001865
DB-057575
MSK001865-1000
N(1,1Dimethylethyl)benzothiazolesulfenamide
2-Benzothiazolesulfenamide,1-dimethylethyl)-
EU-0002407
NS00009355
2Benzothiazolesulfenamide, N(1,1dimethylethyl)
D70664
(1,3-benzothiazol-2-ylsulfanyl)(tert-butyl)amine
1ST001865-1000
AG-690/12868295
N-TERT- BUTYL-2-BENZOTHIAZOLE SULFENAMIDE
SR-01000408154
2-[(tert-Butylamino)sulfanyl]-1,3-benzothiazole #
SR-01000408154-1
Q27292283
(13-BENZOTHIAZOL-2-YLSULFANYL)(TERT-BUTYL)AMINE
Benzothiazolesulfenamide, N-(1,1-dimethylethyl)-(9CI)
N-(1,3-benzothiazol-2-ylthio)-2-methylpropan-2-amine
Solubility of N-(1,3-benzothiazol-2-ylsulfanyl)-2-methyl-propan-2-amine
The solubility of N-(1,3-benzothiazol-2-ylsulfanyl)-2-methyl-propan-2-amine in various solvents can be quite significant due to its unique chemical structure. Its solubility profile can be influenced by various factors, including:
Furthermore, it is essential to consider the following phrases when discussing its solubility:
In conclusion, the solubility of this compound can be a topic of interest, especially in the fields of pharmaceuticals and material sciences, where understanding the dissolution behavior can yield insights into its potential applications.