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Thionobenzophenone

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Identification
Molecular formula
C14H10OS
CAS number
1450-31-3
IUPAC name
S-benzoyl benzenecarbothioate
State
State

At room temperature, thionobenzophenone is typically found in a solid state as a powder within a controlled environment due to its light-sensitive nature. Proper storage conditions help maintain its structural integrity and chemical behavior.

Melting point (Celsius)
62.00
Melting point (Kelvin)
335.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
214.30g/mol
Molar mass
214.3040g/mol
Density
1.1870g/cm3
Appearence

Thionobenzophenone is a solid compound that typically appears as a crystalline powder. It is light-sensitive and should be kept in a light-resistant container. The crystalline form can range in color from light yellow to orange. The color intensity might vary depending on the compound's purity and environmental conditions.

Comment on solubility

Solubility of S-benzoyl benzenecarbothioate

S-benzoyl benzenecarbothioate, a compound known for its distinct structure, exhibits unique solubility characteristics. Understanding its solubility profile is essential for its various applications and chemical behavior.

Solubility Characteristics:

  • Solvent Interaction: S-benzoyl benzenecarbothioate is generally soluble in organic solvents such as ethanol, acetone, and chloroform, which indicates its compatibility with non-polar or slightly polar environments.
  • Water Solubility: This compound has limited solubility in water, primarily due to the hydrophobic nature of the aromatic rings present in its structure.
  • Temperature Dependence: Increased temperatures may enhance its solubility in organic solvents, making it easier to manipulate in various experiments and applications.

It is crucial to note that factors such as pH, temperature, and molecular interactions can significantly influence the solubility of S-benzoyl benzenecarbothioate. As with many chemical compounds, the solubility can also vary with concentration and the presence of other solutes.

In summary, while S-benzoyl benzenecarbothioate shows promising solubility in organic solvents, its limited solubility in water necessitates careful consideration in practical applications.

Interesting facts

Interesting Facts about S-benzoyl benzenecarbothioate

S-benzoyl benzenecarbothioate is a fascinating chemical compound with a variety of interesting properties and applications that any chemistry enthusiast would find captivating. Here are some noteworthy facts:

  • Classification: This compound belongs to the class of thioates, which are known for their sulfur content, providing unique reactivity and characteristics.
  • Applications: S-benzoyl benzenecarbothioate has potential applications in organic synthesis and serves as an intermediate in the production of various agrochemicals and pharmaceuticals.
  • Mechanistic Insight: Its structure is notable for the presence of both carbonyl and thioester groups, making it an ideal candidate for reactions that involve nucleophilic attack. This dual functionality opens up a variety of synthetic pathways.
  • Biological Relevance: Compounds like S-benzoyl benzenecarbothioate often serve as precursors or building blocks for biologically active molecules, adding to their importance in medicinal chemistry.

As you explore the realm of organic compounds, consider the intriguing reactions and transformations that S-benzoyl benzenecarbothioate can undergo. The versatility of its chemical structure invites chemists to innovate and develop new applications, illustrating how diverse and exciting the field of chemistry can be.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." S-benzoyl benzenecarbothioate exemplifies this notion, inspiring chemists to think creatively and push the boundaries of science.

Synonyms
SULFIDE,DIBENZOYL
inchi=1/c14h10o2s/c15-13(11-7-3-1-4-8-11)17-14(16)12-9-5-2-6-10-12/h1-10
Benzoyl sulfide
1850-15-3
Dibenzoyl sulfide
S-benzoyl benzenecarbothioate
Benzoic thioanhydride
Dibenzoic thioanhydride
Benzenecarbothioic acid, anhydrosulfide
BENZOIC ACID, THIO-, ANHYDROSULFIDE
BR7STZ7YMK
NSC-41899
Thiolbenzoic anhydride
NSC 41899
BRN 2050505
Dibenzoylsulfid
AI3-16814
Benzenecarbothioic acid, anhydrosulfide [Czech]
UNII-BR7STZ7YMK
4-09-00-01371 (Beilstein Handbook Reference)
SCHEMBL4453783
DTXSID30171696
NSC41899
AKOS024339781
BENZENECARBOTHIOIC ACID, 1,1'-ANHYDROSULFIDE