N-benzyl-2-methyl-1H-pyrrolo[2,3-d]pyrimidin-4-amine

Identification

Molecular formula

C₁₄H₁₄N₄

CAS number

121507-60-4

IUPAC name

N-benzyl-2-methyl-1H-pyrrolo[2,3-d]pyrimidin-4-amine

State

At room temperature, N-benzyl-2-methyl-1H-pyrrolo[2,3-d]pyrimidin-4-amine is in a solid state. It is typically handled in its powder form and is stable under typical storage conditions.

Melting point (Celsius)

185.00

Melting point (Kelvin)

458.15

Boiling point (Celsius)

330.00

Boiling point (Kelvin)

603.15

General information

Molecular weight

236.28g/mol

Molar mass

236.2800g/mol

Density

1.1900g/cm³

Appearence

N-benzyl-2-methyl-1H-pyrrolo[2,3-d]pyrimidin-4-amine typically appears as a solid crystalline powder. The color of the compound can range from white to off-white, and it may exhibit a slight yellowish tint depending on impurities and synthesis methods.

Comment on solubility

Solubility of N-benzyl-2-methyl-1H-pyrrolo[2,3-d]pyrimidin-4-amine

N-benzyl-2-methyl-1H-pyrrolo[2,3-d]pyrimidin-4-amine is a fascinating compound that showcases interesting solubility characteristics. The solubility of this compound can be influenced by several factors:

Polarity: The presence of both benzyl and methyl groups affects the overall polarity of the molecule, contributing to its interactions with solvents.
Solvent Type: Typically, this compound may show better solubility in organic solvents such as dimethyl sulfoxide (DMSO) or dimethylformamide (DMF) compared to polar solvents like water.
Temperature: As with many organic compounds, increased temperature generally enhances solubility. Thus, heating solvents might facilitate the dissolution process.
Hydrogen Bonding: The presence of amine functional groups can engage in hydrogen bonding, which may enhance solubility in certain solvents while creating barriers in others.

In summary, while N-benzyl-2-methyl-1H-pyrrolo[2,3-d]pyrimidin-4-amine may exhibit varying degrees of solubility depending on the environmental conditions, its overall behavior suggests a preference for organic media over aqueous solutions. Understanding these solubility dynamics is crucial for practical applications in drug formulation and chemical synthesis.

Interesting facts

Interesting Facts about N-benzyl-2-methyl-1H-pyrrolo[2,3-d]pyrimidin-4-amine

N-benzyl-2-methyl-1H-pyrrolo[2,3-d]pyrimidin-4-amine is a fascinating organic compound that presents numerous avenues for research and application within the realm of chemistry and pharmacology. Here are some intriguing aspects of this compound:

Structural Diversity: This compound features a unique fusion of a pyrrole and a pyrimidine ring, showcasing a blend of nitrogen heterocycles that can exhibit distinct electronic properties.
Potential Biological Activity: Compounds with similar structures have been explored for their biological activities, including potential antifungal, antiviral, and anticancer properties. Studying N-benzyl-2-methyl-1H-pyrrolo[2,3-d]pyrimidin-4-amine could unveil novel therapeutic pathways.
Synthetic Routes: The synthesis of pyrrolo[2,3-d]pyrimidines often involves multi-step reactions that can include strategies like cyclization and functionalization, making it a captivating subject for synthetic chemists.
Research Implications: As researchers continue to uncover the functionalities of nitrogen-containing compounds, this specific derivative may serve as a valuable lead compound for designing more effective drugs.

Overall, N-benzyl-2-methyl-1H-pyrrolo[2,3-d]pyrimidin-4-amine exhibits properties that warrant further investigation, making it an exciting focus for chemists and biologists alike. The phrase "exploration of the unknown" resonates with scientists who seek to delve into the complex interactions of such novel compounds that blend organic structure with potential biological applications.