Interesting facts
Overview of 1-(1,3-benzothiazol-2-yl)-1,3-dimethyl-urea
1-(1,3-benzothiazol-2-yl)-1,3-dimethyl-urea is an intriguing compound that has captured the attention of researchers for its unique properties and potential applications. This compound belongs to a class of chemicals known as ureas, which are characterized by a carbonyl group attached to a nitrogen atom.
Interesting Facts
- Biological Significance: This compound has been studied for its potential antimicrobial properties, making it a subject of interest in medicinal chemistry. It might pave the way for new antibacterial agents that could combat resistant strains of bacteria.
- Versatile Applications: Beyond its use in pharmaceuticals, 1-(1,3-benzothiazol-2-yl)-1,3-dimethyl-urea could have applications in agricultural chemistry as a plant growth regulator. Its structural similarity to enzymes may allow it to interact with biological systems in unique ways.
- Structure-Activity Relationship: The presence of the benzothiazole moiety might enhance its biological activity compared to other urea derivatives. This relationship is crucial in drug design, where small changes in chemical structure can lead to significant differences in efficacy.
- Research Opportunities: Ongoing studies are examining how this compound can be used as a starting point to synthesize more complex structures, potentially leading to new therapeutic compounds with improved effectiveness.
- Environmental Impact: Understanding the environmental behavior of this compound is vital, especially if it is used widely in agriculture. Investigating its degradation pathways can help assess its environmental footprint and guide safe usage.
As research unfolds, 1-(1,3-benzothiazol-2-yl)-1,3-dimethyl-urea stands as a beacon of potential in various fields, from environmental science to pharmaceuticals. Its multifaceted nature illustrates the beauty of chemistry in creating compounds that hold promise for future innovations. As one researcher aptly put it, "The real magic of chemistry lies in its ability to transform simple molecules into powerful tools for change."
Synonyms
Methabenzthiazuron
18691-97-9
Metabenzthiazuron
TRIBUNIL
Bayer 5633
1-(2-Benzothiazolyl)-1,3-dimethylurea
N-2-Benzothiazolyl-N,N'-dimethylurea
Bayer 74283
82NPF43P0X
DTXSID0037570
TRIBUNIL (BAYER)
1-(1,3-benzothiazol-2-yl)-1,3-dimethyl-urea
N-(2-Benzothiazolyl)-N,N'-Dimethylurea
DTXCID8017570
242-505-0
Methbenzthiazuron
Preparation 5633
1-(1,3-benzothiazol-2-yl)-1,3-dimethylurea
1,3-Dimethyl-3-(2-benzothiazolyl)urea
Urea, N-2-benzothiazolyl-N,N'-dimethyl-
BAY 74283
Urea, 1-(2-benzothiazolyl)-1,3-dimethyl-
N-Methyl-N'-methyl-N'-(2-benzothiazolyl)urea
CHEBI:6803
1,3-Dimethyl-3-(2-benzthiazolyl)-harnstoff
MFCD00055498
Methabenzthiazuron 10 microg/mL in Acetonitrile
Methabenzthiazuron 100 microg/mL in Acetonitrile
Caswell No. 081B
Methabenzthiazuron [BSI:ISO]
CCRIS 6766
1-(Benzothiazol-2-yl)-1,3-dimethylurea
Methabenzthiazuron [ISO]
EINECS 242-505-0
EPA Pesticide Chemical Code 281300
BRN 0196633
UNII-82NPF43P0X
1-Benzothiazol-2-yl-1,1'-dimethylurea
Methibenzuron
Methabenzthiazuro
S 25128
1,3-Dimethyl-3-(2-benzthiazolyl)-harnstoff [German]
Bayer 5653
SCHEMBL66434
4-27-00-04842 (Beilstein Handbook Reference)
METHABENZTHIAZURON [MI]
Bay 72483
CHEMBL1890813
SCHEMBL29549492
RRVIAQKBTUQODI-UHFFFAOYSA-
BAY 5653
Tox21_300966
AKOS015913141
(Benzothiazol-2-yl)-1,3-dimethylurea
HY-W414724
NCGC00163728-01
NCGC00163728-02
NCGC00254869-01
BS-44136
CAS-18691-97-9
M2334
NS00010463
D91591
A813097
N-(1,3-Benzothiazol-2-yl)-N,N'-dimethylurea #
Methabenzthiazuron, PESTANAL(R), analytical standard
Q15632903
InChI=1/C10H11N3OS/c1-11-9(14)13(2)10-12-7-5-3-4-6-8(7)15-10/h3-6H,1-2H3,(H,11,14)
Solubility of 1-(1,3-benzothiazol-2-yl)-1,3-dimethyl-urea
1-(1,3-benzothiazol-2-yl)-1,3-dimethyl-urea exhibits interesting solubility characteristics influenced by its molecular structure. Here are some key points regarding its solubility:
In practice, understanding the solubility of 1-(1,3-benzothiazol-2-yl)-1,3-dimethyl-urea is essential for its application in various fields, such as pharmaceuticals and agrochemicals. As with many compounds, the statement “solubility is a key aspect of reactivity” holds true, highlighting the importance of studying this property in-depth.