Interesting facts
Interesting Facts about S-benzyl benzenecarbothioate
S-benzyl benzenecarbothioate is a fascinating compound known for its unique chemical properties and its applications in various fields. As a thioester, it plays a significant role in organic synthesis and has garnered attention in recent research. Here are some intriguing aspects of this compound:
- Thioester Group: The presence of the thioester functional group makes S-benzyl benzenecarbothioate reactive and useful in the formation of new chemical bonds, particularly in synthetic organic chemistry.
- Potential Applications: This compound can be utilized in the development of pharmaceuticals and agricultural chemicals, contributing to the advancement of both fields.
- Reactivity: S-benzyl benzenecarbothioate can undergo various reactions, including hydrolysis and transesterification, making it a versatile compound in chemical reactions.
- Research Insights: Studies have indicated that compounds similar to S-benzyl benzenecarbothioate may exhibit interesting biological activities, paving the way for further exploration of their medicinal properties.
- Environmental Considerations: Understanding the behavior of this compound in different environments is essential, especially when considering its impact on ecosystems and potential for biodegradation.
In summary, S-benzyl benzenecarbothioate is not only a significant player in organic synthesis but also a compound that opens doors to new research and applications. Its thioester structure and potential uses make it a subject worthy of study in both academic and industrial settings.
Synonyms
Tibenzate
S-Benzyl benzenecarbothioate
13402-51-2
Benzyl thiobenzoate
Tibenzate [INN]
Tibenzato
S-Benzyl thiobenzoate
Benzenecarbothioic acid, S-(phenylmethyl) ester
NSC-79263
0I93JSA6L6
S-Benzyl benzothioate
Tibenzatum
Thiobenzoic acid, S-benzyl ester
Tibenzatum [INN-Latin]
Tibenzato [INN-Spanish]
NSC 79263
alpha-Toluenethiol, benzoate
BRN 2049281
UNII-0I93JSA6L6
AI3-16937
BENZOIC ACID, THIO-, S-BENZYL ESTER
WLN: RVS1R
phenyl phenylmethylthio ketone
Benzoic acid, S-benzyl ester
SCHEMBL2110094
SCHEMBL7304143
Thiobenzoic acid S-benzyl ester
CHEMBL2107077
(benzylsulfanyl)(phenyl)methanone
DTXSID90158463
s-(Phenylmethyl)benzenecarbothioate
NSC79263
STK822760
AKOS002346585
SDCCGSBI-0660758.P001
NS00122412
ST45247775
SR-01000884008
SR-01000884008-1
Q27236811
Solubility of S-benzyl benzenecarbothioate
S-benzyl benzenecarbothioate is a compound that exhibits varying solubility characteristics depending on the solvent used. Generally, it has a moderate to low solubility in water, primarily due to its hydrophobic aromatic structure. However, it is more soluble in organic solvents. The solubility profile can be outlined as follows:
As a rule of thumb in chemistry, "like dissolves like," meaning that polar solutes tend to dissolve best in polar solvents, while non-polar solutes are better suited to non-polar solvents. Thus, the solubility of S-benzyl benzenecarbothioate demonstrates this principle clearly.
In conclusion, understanding the solubility of this compound is critical for its application in various chemical processes and formulations. Knowledge of its solubility behavior can influence choices in synthesis and extraction techniques.