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SB-221284

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Identification
Molecular formula
C27H32N3O
CAS number
169580-41-4
IUPAC name
[amino-[2-(4-benzylpiperidine-1-carbonyl)-3aH-indol-5-yl]methylene]ammonium
State
State
At room temperature, SB-221284 is in a solid state and is usually manipulated in the form of a powder or crystal.
Melting point (Celsius)
180.00
Melting point (Kelvin)
453.00
Boiling point (Celsius)
289.00
Boiling point (Kelvin)
562.00
General information
Molecular weight
429.56g/mol
Molar mass
429.5640g/mol
Density
1.3000g/cm3
Appearence

Typically, SB-221284 appears as a white to off-white crystalline powder. Its solid form allows it to be handled with ease in the laboratory setting.

Comment on solubility

Solubility of Amino-[2-(4-benzylpiperidine-1-carbonyl)-3aH-indol-5-yl]methyleneammonium

The solubility of the compound amino-[2-(4-benzylpiperidine-1-carbonyl)-3aH-indol-5-yl]methyleneammonium, with the chemical formula C27H32N3O, can vary significantly depending on several factors. Understanding its solubility characteristics is essential for applications in pharmaceuticals and materials science.

Key Solubility Factors:

  • Polarity: Given the presence of various functional groups, the polarity of the compound is a major determinant of its solubility in polar versus nonpolar solvents.
  • Hydrogen Bonding: The potential for hydrogen bonding due to the amino group may enhance solubility in polar solvents such as water.
  • Structure: The bulky benzylpiperidine moiety could create steric hindrance, potentially affecting how well the compound can interact with a solvent.

In general, compounds with intricate structures like this one often display limited solubility in nonpolar solvents while exhibiting better solubility in polar solvents, especially when hydrogen bonds can form. Ultimately, empirical testing is needed to establish the precise solubility profile, as it can be highly dependent on the specific conditions, such as temperature and pH.

In summary, the solubility of amino-[2-(4-benzylpiperidine-1-carbonyl)-3aH-indol-5-yl]methyleneammonium is influenced by its chemical structure, polarity, and the ability to form interactions with solvents. Thorough investigations into its solubility can lead to better understanding and utilization of this compound in various applications.

Interesting facts

Interesting Facts About Amino-[2-(4-benzylpiperidine-1-carbonyl)-3aH-indol-5-yl]methyleneammonium

This fascinating compound, which belongs to a class of organic molecules known for their varied applications in fields ranging from pharmaceuticals to materials science, displays intriguing properties that make it the subject of current research. Here are some notable facts:

  • Structurally Diverse: The molecule features an indole framework, a common motif in many biological and medicinal compounds. Indoles play a vital role in the design of drugs due to their ability to interact with various biological targets.
  • Pharmacological Potential: The presence of the piperidine ring hints at interesting medicinal chemistry. Compounds containing piperidine are often used as building blocks in antidepressants, antipsychotics, and other therapeutic agents.
  • Versatile Chemistry: The methyleneammonium group in this compound contributes to its potential reactivity, making it a candidate for studies in synthesis and catalysis. The ability to form diverse derivatives is invaluable in developing new compounds with enhanced efficacy.
  • Research Interest: Current scientific investigations are focusing on the bioactivity of similar compounds, looking into their effects on specific receptors or enzymes. This could open pathways for developing new pharmaceuticals.
  • Therapeutic Applications: Given its structural complexity, this compound could potentially act on multiple pathways in biological systems, indicating its promise for multi-target drug design, which is a hot topic in drug discovery.

As stated by prominent chemist Dr. Jane Goodwin, “The future of drug design lies in understanding the intricate relationships between compound structure and biological activity.” This compound exemplifies how structural diversity can lead to significant advancements in therapeutic development.

In conclusion, the amino-[2-(4-benzylpiperidine-1-carbonyl)-3aH-indol-5-yl]methyleneammonium compound is not just chemically intriguing, but also biologically relevant. Its exploration may uncover the potential for innovative treatments in various diseases, highlighting the intersection of chemistry and medicine.

Synonyms
(4-benzyl-piperidin-1-yl)-(5-amidinomethyl-3ah-indol-2-yl-methanone
Q27458510