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Benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate

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Identification
Molecular formula
C22H21N3O3
CAS number
137792-28-8
IUPAC name
benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate
State
State

At room temperature, the compound is in a solid state. It is typically found in a stable crystalline form and should be stored in a cool, dry location to maintain its integrity.

Melting point (Celsius)
162.00
Melting point (Kelvin)
435.15
Boiling point (Celsius)
515.30
Boiling point (Kelvin)
788.45
General information
Molecular weight
348.42g/mol
Molar mass
348.3850g/mol
Density
1.2896g/cm3
Appearence

Benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate typically appears as a white to off-white powder. It is crystalline in nature and can be handled as a fine powder or larger crystal aggregates.

Comment on solubility

Solubility of Benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate

The solubility of benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate (C22H21N3O3), a complex organic molecule, can be influenced by several factors, including polarity, molecular structure, and the nature of the solvent. Here are some key points to consider:

  • Polarity: The presence of both hydrophilic (polar) and hydrophobic (non-polar) regions in the molecule suggests that its solubility may vary greatly in different solvents.
  • Solvent Characteristics: Benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate is likely to be more soluble in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), and acetone, which can effectively solvate polar and non-polar functional groups.
  • Temperature Influence: Like many organic compounds, its solubility may increase with temperature, allowing for better dissolution in higher temperatures compared to lower ones.

That being said, quantifying the exact solubility can be challenging and often requires empirical testing. As a general guideline, compounds with similar functional groups typically yield better solubility patterns. Therefore, experimenting under controlled conditions would be beneficial for precise solubility data.

In conclusion, while the solubility profile of benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate is complex and highly dependent on the solvent employed, understanding these underlying factors can lead to effective applications in various fields, including pharmaceuticals and chemical synthesis.

Interesting facts

Interesting Facts about Benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate

Benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate is a fascinating compound that holds significant interest in the realms of medicinal chemistry and organic synthesis. Here are some key points that highlight its importance:

  • Medicinal Applications: This compound is known for its potential therapeutic applications, particularly in cancer treatment. Its structure allows for interaction with various biological targets, making it a candidate for further research in pharmacology.
  • Complex Structure: The intricate arrangement of functional groups in benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate showcases the beauty of organic chemistry. The presence of multiple aromatic rings indicates that it may exhibit unique electronic properties.
  • Synthesis Pathways: The synthesis of this compound often involves multi-step reactions, providing students with a practical example of how complex organic molecules can be constructed in the laboratory. Understanding its synthesis can offer insights into reaction mechanisms, such as acylation and amidation.
  • Structure-Activity Relationship (SAR): Researchers utilize compounds like this one to explore the SAR, helping to establish how modifications to the molecular structure can influence biological activity. This is crucial for designing more effective drugs with fewer side effects.
  • Interdisciplinary Connections: The study of benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate intersects with various fields including neuroscience, medicinal chemistry, and materials science, making it a great topic for interdisciplinary studies.

In summary, benzyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate is not just a compound; it represents the culmination of intricate chemical design and potential real-world applications. As noted by many chemists, "The beauty of chemistry lies in its ability to transform small molecules into agents of change." This compound embodies that beauty.

Synonyms
CHEMBL357268
N-(2-Aminophenyl)-4-[N-(pyridine-3-ylmethoxycarbonyl)aminomethyl]benzamide
209783-81-3
Phenylmethyl N-[[4-[[(2-aminophenyl)amino]carbonyl]phenyl]methyl]carbamate
Phenylmethyl N-((4-(((2-aminophenyl)amino)carbonyl)phenyl)methyl)carbamate
HDInhib_000007
SCHEMBL2410629
UZCQCEODMVDIJR-UHFFFAOYSA-N
DTXSID001145786
BDBM50474342
benzyl {4-[(2-aminophenyl)carbamoyl]benzyl}carbamate