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Carbamothioic acid, diphenyl-, S-[2-(diethylamino)ethyl] ester

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Identification
Molecular formula
C19H24N2OS
CAS number
977-42-8
IUPAC name
S-[2-(diethylamino)ethyl] N,N-diphenylcarbamothioate
State
State

At room temperature, S-[2-(diethylamino)ethyl] N,N-diphenylcarbamothioate is typically found in a solid state.

Melting point (Celsius)
58.00
Melting point (Kelvin)
331.15
Boiling point (Celsius)
425.00
Boiling point (Kelvin)
698.15
General information
Molecular weight
344.52g/mol
Molar mass
344.5210g/mol
Density
1.1200g/cm3
Appearence

This compound typically appears as a yellow to off-white crystalline solid.

Comment on solubility

Solubility of S-[2-(diethylamino)ethyl] N,N-diphenylcarbamothioate

S-[2-(diethylamino)ethyl] N,N-diphenylcarbamothioate, with the chemical formula C19H24N2OS, has some unique properties when it comes to solubility. Understanding the solubility characteristics of this compound is crucial for its applications in various fields.

In general, the solubility of organic compounds like this one can be influenced by several key factors:

  • Polarity: The presence of polar groups in the molecule can increase solubility in polar solvents, while non-polar sections may favor solubility in non-polar solvents.
  • Hydrogen bonding: Compounds that can participate in hydrogen bonding typically demonstrate higher solubility in water or other polar solvents.
  • Substituent effects: The diethylamino group adds some degree of polarity, which may enhance solubility in polar environments.

For S-[2-(diethylamino)ethyl] N,N-diphenylcarbamothioate, one might expect:

  • A moderate solubility in organic solvents such as ethanol and acetone.
  • Possibly limited solubility in water due to its overall molecular structure.
  • Enhanced solubility in mixed solvent systems that can balance both polar and non-polar characteristics.

As the saying goes, "Like dissolves like", and therefore, when working with this compound, suitable solvents should be chosen to improve dissolution and ensure effective usage in chemical processes.

In conclusion, while the exact solubility of S-[2-(diethylamino)ethyl] N,N-diphenylcarbamothioate might require further experimental determination, considering the above factors will provide a useful starting point for understanding its behavior in various solvents.

Interesting facts

Interesting Facts about S-[2-(diethylamino)ethyl] N,N-diphenylcarbamothioate

S-[2-(diethylamino)ethyl] N,N-diphenylcarbamothioate is a fascinating compound belonging to the class of carbamates, which are known for their diverse applications in various scientific fields. Here are some intriguing aspects of this compound:

  • Pharmacological Potential: Compounds like S-[2-(diethylamino)ethyl] N,N-diphenylcarbamothioate are studied for their potential pharmacological properties, often serving as prototypes for developing new pharmaceuticals.
  • Structure-Activity Relationship: Investigating the structural elements of this compound can provide insights into how modifications can enhance or reduce biological activity, an essential aspect of medicinal chemistry.
  • Synthesis and Reactivity: The synthesis of carbamothioates generally involves nucleophilic attack on carbonyl compounds, making them interesting targets for organic synthesis and reactivity studies.
  • Toxicology Studies: Given the presence of a thiocarbamate moiety, the compound is also relevant in toxicology and environmental studies, where it may be essential to assess its toxicity and environmental impact.
  • Versatile Applications: Carbamates have found their way into various applications, including agrochemicals, polymers, and insecticides, highlighting the versatility of compounds with thiourea functionality.
  • Historical Context: The study of carbamates has a rich history dating back to the early 19th century, marking an essential milestone in the development of organic chemistry.

As a compound that exemplifies the intersection of organic chemistry and pharmacology, S-[2-(diethylamino)ethyl] N,N-diphenylcarbamothioate indeed underscores the importance of chemical compounds in advancing scientific knowledge and practical applications.

Synonyms
Phencarbamide
Fencarbamide
3735-90-8
Phencarbamid
Escorpal
Rispasulf
Phencarbamide [USAN]
Fencarbamida
Bayer 1355
Fencarbamidum [INN-Latin]
Fencarbamida [INN-Spanish]
Fencarbamide [INN]
BAY 1355
EINECS 223-103-4
Escorpal (TN)
UNII-59H17J9F1B
BRN 2753271
Fencarbamide (INN)
Phencarbamide (USAN)
S-[2-(diethylamino)ethyl] N,N-diphenylcarbamothioate
S-(2-(Diethylamino)ethyl) diphenylthiocarbamate
PHENCARBAMIDE [MI]
Carbamothioic acid, diphenyl-, S-(2-(diethylamino)ethyl) ester
FENCARBAMIDE [MART.]
FENCARBAMIDE [WHO-DD]
DTXSID80190796
59H17J9F1B
CARBAMIC ACID, DIPHENYLTHIO-, S-(2-(DIETHYLAMINO)ETHYL) ESTER
Escorpal; Fencarbamide; Phencarbamid; Rispasulf
Fencarbamidum (INN-Latin)
Fencarbamida (INN-Spanish)
FENCARBAMIDE (MART.)
Fencarbamidum
S-[2-(Diethylamino)ethyl] diphenylthiocarbamate
Diphenylthiocarbamic acid S-(2-(diethylamino)ethyl) ester
SCHEMBL249495
CHEMBL2107472
DTXCID20113287
BZGIPVGCJGXQTA-UHFFFAOYSA-N
NS00045790
D05452
Q27261706