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Tiodazosin

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Identification
Molecular formula
C26H38N4O6S2
CAS number
75507-68-5
IUPAC name
isopropyl 2-[[2-[2-[(2-amino-3-sulfanyl-propyl)amino]-3-methyl-pentoxy]-3-phenyl-propanoyl]amino]-4-methylsulfonyl-butanoate
State
State
At room temperature, Tiodazosin is a solid. It is usually handled as a powder and stored in a sealed container to prevent it from absorbing moisture from the air.
Melting point (Celsius)
149.00
Melting point (Kelvin)
422.15
Boiling point (Celsius)
642.15
Boiling point (Kelvin)
915.30
General information
Molecular weight
565.73g/mol
Molar mass
565.7330g/mol
Density
1.3280g/cm3
Appearence

Tiodazosin typically appears as a white to off-white powder. It is a chemical compound known for its pharmaceutical applications, particularly as an adrenergic blocker used in medical treatments.

Comment on solubility

Solubility of Isopropyl 2-[[2-[2-[(2-amino-3-sulfanyl-propyl)amino]-3-methyl-pentoxy]-3-phenyl-propanoyl]amino]-4-methylsulfonyl-butanoate

The solubility of this complex compound, C26H38N4O6S2, is influenced by various factors due to its intricate chemical structure. Here are some key points to consider about its solubility:

  • Polarity: The presence of multiple polar functional groups, such as the sulfonyl and amino groups, suggests that this compound may have a decent affinity for polar solvents like water.
  • Hydrophobic Regions: The hydrocarbon chains in its structure can lead to hydrophobic interactions, which may decrease its overall solubility in polar solvents.
  • Solvent Systems: It could be more soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO) compared to water, as these solvents can better accommodate its bulky, nonpolar parts.
  • Temperature Effects: As is typical with many compounds, solubility may increase with temperature, revealing the dynamic nature of solubility behavior.

In summary, while the overall polarity suggests some level of solubility in polar solvents, the compound’s hydrophobic components and multivalency must be considered to predict its behavior accurately in different solvent systems. Ultimately, experimental evidence would provide the most reliable insights into its solubility profile.

Interesting facts

Interesting Facts about Isopropyl 2-[[2-[2-[(2-amino-3-sulfanyl-propyl)amino]-3-methyl-pentoxy]-3-phenyl-propanoyl]amino]-4-methylsulfonyl-butanoate

This compound, known as isopropyl 2-[[2-[2-[(2-amino-3-sulfanyl-propyl)amino]-3-methyl-pentoxy]-3-phenyl-propanoyl]amino]-4-methylsulfonyl-butanoate, is a fascinating example of the complexity of modern pharmaceuticals and biochemistry. It exemplifies how intricate chemical designs can yield compounds that may have significant therapeutic potential.

Key Features:

  • Multi-Functional Structure: The compound consists of multiple functional groups that lend specific properties, which may enhance bioactivity.
  • Involvement in Pharmaceutical Research: Its unique moieties make it a subject of interest in drug development, particularly for targeting various biological pathways.
  • Potential for Therapeutic Applications: Given its amino and sulfonyl groups, it may have implications in treating various conditions by influencing enzyme activity or cellular signaling.
  • Chemical Diversity: Composed of carbon, hydrogen, nitrogen, oxygen, and sulfur atoms, the variety of elements reflects its comprehensive chemical potential.

In summary, as a compound of notable architectural complexity, it is a prime example of the intersection of chemistry and medicine. Its design reflects the careful planning and synthesis needed to create compounds that not only fulfill therapeutic roles but also provide insight into biochemical pathways.

To quote a well-known chemist, "Nature is a source of inspiration for the design of novel compounds, and this one certainly showcases the beauty of chemical engineering."

Synonyms
(2S)-[(2S)-[(2R)-Amino-3-mercapto]-propylamino-(3S)-methyl]pentyloxy-3-phenylpropionyl-methionine Sulfone Isopropyl Ester Bis Hydrchloride
L-744832
SCHEMBL8257212
(2S)-2-[[2-[(2S,3S)-2-[[(2R)-2-amino-3-mercaptopropyl]amino]-3-methylpentoxy]-1-oxo-3-phenylpropyl]amino]-4-methylsulfonylbutanoic acid propan-2-yl ester
propan-2-yl 2-[[2-[2-[(2-amino-3-sulfanylpropyl)amino]-3-methylpentoxy]-3-phenylpropanoyl]amino]-4-methylsulfonylbutanoate
L-744 832