Interesting facts
Exploring S-(2-benzamidophenyl) benzenecarbothioate
S-(2-benzamidophenyl) benzenecarbothioate is a fascinating compound that showcases the intricate world of organic chemistry. This compound is an example of a thioester, which is characterized by the presence of a sulfur atom bonded to a carbonyl group. Here are some intriguing facts about this compound:
- Background: This thioester features a benzamide moiety, which adds complexity to its structure and may influence its chemical behavior and biological activities.
- Reactivity: Thioesters, such as S-(2-benzamidophenyl) benzenecarbothioate, are known to be highly reactive. They participate in a range of chemical reactions, including nucleophilic acyl substitution, which can lead to further derivatization.
- Applications: Due to its unique structure, this compound may have potential applications in medicinal chemistry. Research is ongoing to explore its properties in drug development, particularly as a scaffold for creating bioactive molecules.
- Analogous Compounds: S-(2-benzamidophenyl) benzenecarbothioate is related to other thioesters and amide compounds that are vital in various biochemical pathways, demonstrating the interconnectedness of organic compounds.
- Importance in Synthesis: This compound can be utilized as a key intermediate in the synthesis of more complex organic structures, making it a valuable asset for synthetic chemists.
As a testament to the beauty of chemical diversity, compounds like S-(2-benzamidophenyl) benzenecarbothioate remind us of the innovative paths that scientific research can take. Each molecule has its own story, and understanding these compounds not only reveals their unique characteristics but also their potential to contribute to advancements in various fields.
Synonyms
Benzanilide, 2'-benzoylthio-
1047-61-6
S-(2-benzamidophenyl) benzenecarbothioate
N,S-Dibenzoyl-o-aminothiofenol
N,S-Dibenzoyl-o-aminothiophenol
BENZOIC ACID, THIO-, o-BENZAMIDOPHENYL ESTER
MLS003115173
0TSY2M49G0
Thiobenzoic acid S-[2-(benzoylamino)phenyl] ester
NSC-234309
Benzenecarbothioic acid, S-(2-(benzoylamino)phenyl) ester
Benzenecarbothioic acid, S-[2-(benzoylamino)phenyl] ester
NSC 234309
BRN 2221593
N,S-Dibenzoyl-o-aminothiofenol [Czech]
PEPTAZIN BFT
UNII-0TSY2M49G0
3-13-00-00916 (Beilstein Handbook Reference)
CHEMBL1873372
DTXSID10146660
S-(2-Benzamidophenyl) benzothioate
NSC234309
STK331123
Benzoic acid, o-benzamidophenyl ester
AKOS004909841
N,S-DIBENZOYL-2-AMINOTHIOPHENOL
SMR001830756
BENZANILIDE, 2'-MERCAPTO-, BENZOATE
S-{2-[(phenylcarbonyl)amino]phenyl} benzenecarbothioate
BENZOIC ACID, THIO-, S-ESTER WITH 2'-MERCAPTOBENZANILIDE
Solubility of S-(2-benzamidophenyl) benzenecarbothioate
S-(2-benzamidophenyl) benzenecarbothioate is a complex compound whose solubility characteristics can be influenced by several factors. Understanding its solubility in various solvents is key for applications in chemical synthesis and formulation. Here are some critical aspects to consider:
In summary, while the exact solubility of S-(2-benzamidophenyl) benzenecarbothioate may not be readily available, factors such as solvent polarity, temperature, pH, and the potential use of co-solvents are crucial for optimizing its dissolution in laboratory settings. As with many chemical compounds, empirical testing will be vital to ascertain its true solubility profile.