Interesting facts
Interesting Facts about S-benzoylsulfanyl benzenecarbothioate
S-benzoylsulfanyl benzenecarbothioate is a fascinating compound that belongs to the class of organosulfur compounds. Here are some noteworthy aspects about this intriguing molecule:
- Functional Groups: The compound contains both a benzothioate group and sulfenyl groups. The presence of these functional groups contributes to its unique reactivity and potential applications in organic synthesis.
- Synthesis: S-benzoylsulfanyl benzenecarbothioate can be synthesized through a series of chemical reactions involving thioacids and benzoyl derivatives. This synthesis pathway showcases the versatility of sulfur chemistry.
- Applications: Organosulfur compounds like S-benzoylsulfanyl benzenecarbothioate are essential in many fields, including pharmaceuticals and agrochemicals. They are often studied for their potential roles as intermediates in the synthesis of biologically active molecules.
- Biological Activity: Research indicates that organosulfur compounds can exhibit various biological activities, including antimicrobial and antifungal properties, making compounds like S-benzoylsulfanyl benzenecarbothioate a point of interest in medicinal chemistry.
- Chemical Behavior: The compound's structure allows for interesting reactivity patterns. For instance, the thiol group can participate in nucleophilic substitution reactions, potentially leading to a range of derivatives with enhanced properties.
As a conclusion, S-benzoylsulfanyl benzenecarbothioate exemplifies the richness of organosulfur chemistry, offering numerous possibilities for exploration and innovation in both academic and industrial contexts. Its study highlights the importance of functionalization in creating new compounds with desirable qualities.
Synonyms
Benzoyl disulfide
644-32-6
Dibenzoyl disulphide
Disulfide, dibenzoyl
Bensulfenum
Benthiolan
Dibenzoyl disulfide
Septiolan
Thiocutol
BENZENE, DITHIODICARBONYLDI-
NSC 209
EINECS 211-413-2
NSC 677460
NSC-677460
BRN 1114144
AI3-03083
NSC-209
XO5F8186C4
DTXSID40214649
3-09-00-01977 (Beilstein Handbook Reference)
Benzoyl disulfide (6CI,7CI,8CI)
Disulfide, dibenzoyl (9CI)
DTXCID20137140
S-benzoylsulfanyl benzenecarbothioate
Benzoic dithioperoxyanhydride
benzenecarbothioic acid S-(benzoylthio) ester
NSC677460
DISULFIDE,DIBENZOYL
UNII-XO5F8186C4
WLN: RVSSVR
SCHEMBL168007
CHEMBL120631
NSC209
YYWLHHUMIIIZDH-UHFFFAOYSA-N
(benzoyldisulfanyl)(phenyl)methanone
AAA64432
STK293204
AKOS015917333
BS-48949
NS00035697
F73035
Q27293930
InChI=1/C14H10O2S2/c15-13(11-7-3-1-4-8-11)17-18-14(16)12-9-5-2-6-10-12/h1-10
Solubility of S-benzoylsulfanyl benzenecarbothioate
S-benzoylsulfanyl benzenecarbothioate, a compound known for its unique structure, exhibits selective solubility characteristics. Understanding its solubility can provide insight into its behavior in various solvents and environmental conditions.
Key Points on Solubility:
In summary, the solubility of S-benzoylsulfanyl benzenecarbothioate is influenced by its molecular structure and the properties of the solvent. When considering its practical applications, it is essential to select the appropriate solvent to optimize its solubility characteristics.