Interesting facts
Interesting Facts about 1-bromo-4-isothiocyanato-benzene
1-bromo-4-isothiocyanato-benzene is a fascinating compound that combines elements of both aromatic and functional group chemistry. Here are some engaging aspects worth noting:
- Versatile Intermediate: This compound is frequently employed as an intermediate in organic synthesis. It can lead to the development of various useful derivatives by undergoing nucleophilic substitution reactions.
- Biological Relevance: Interestingly, isothiocyanates are known for their biological activities. They have been the subject of research for their potential anti-cancer properties. The compound's structure has led scientists to investigate its effects on various cancer cell lines.
- Industrial Applications: In addition to its significance in research, this compound finds its applications in the formulation of herbicides and pesticides. Its effectiveness in controlling pests makes it valuable in agricultural chemistry.
- Teaching Tool: Due to its unique structure featuring both a bromine atom and an isothiocyanate group, this compound is often used in teaching scenarios to illustrate concepts such as substitution reactions and the reactivity of aromatic compounds.
- Reaction Diversity: Being part of the aromatic family, it exhibits the typical reactivity patterns associated with benzene derivatives, allowing for a wide range of chemical reactions including electrophilic aromatic substitution and nucleophilic cyclization.
In summary, the compound 1-bromo-4-isothiocyanato-benzene serves not only as a pivotal chemical in research and industrial applications, but also as a robust subject of study that bridges multiple areas of chemistry. Its properties and potential make it a compound of interest for both budding chemists and seasoned professionals.
Synonyms
4-Bromophenyl isothiocyanate
1985-12-2
Benzene, 1-bromo-4-isothiocyanato-
1-Bromo-4-isothiocyanatobenzene
4-Bromophenylisothiocyanate
Trichofytocid
p-Bromophenyl isothiocyanate
Bromobenzene-4-isothiocyanate
RIT5DF1B5G
ISOTHIOCYANIC ACID, p-BROMOPHENYL ESTER
TRICHOPHYTOCID
NSC 72012
NSC-72012
p-Bromophenylisothiocyanate
4-bromophenyl-isothiocyanate
BRN 0878549
AI3-16039
DTXSID30173594
DTXCID8096085
628-470-8
inchi=1/c7h4brns/c8-6-1-3-7(4-2-6)9-5-10/h1-4
MFCD00004808
Isothiocyanic Acid 4-Bromophenyl Ester
WLN: SCNR DE
UNII-RIT5DF1B5G
p-Bromphenyl-iso-thiocyanat
NCIOpen2_003623
4-bromo phenyl isothiocyanate
Phenylisothiocyanate, 4-bromo
(4-bromo-phenyl)isothiocyanate
SCHEMBL1019382
1-isothiocyanato-4-bromobenzene
1-bromo-4-isothio-cyanatobenzene
1-bromo-4-isothiocyanato-benzene
1-Bromo-4-isothiocyanatobenzene #
4-Bromophenyl isothiocyanate, 97%
NSC72012
STL197856
AKOS000212188
FS-3858
BP-12927
SY001061
DB-045007
I0526
EN300-24199
F20971
F1915-0004
Solubility of 1-bromo-4-isothiocyanato-benzene
The compound 1-bromo-4-isothiocyanato-benzene possesses unique solubility characteristics that warrant attention. Its solubility can be influenced by several factors, including its polar and nonpolar functional groups, as well as temperature and solvent type.
Factors Affecting Solubility:
In summary, while 1-bromo-4-isothiocyanato-benzene can exhibit solubility in various organic solvents, its behavior is primarily governed by its polarity and the nature of the solvent. The most effective approach for maximizing solubility involves selecting the right solvent and conditions.