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Bambuterol

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Identification
Molecular formula
C18H29N2O5
CAS number
81732-46-9
IUPAC name
2-[2-(2-ethoxy-3-methoxy-phenyl)ethyl-[2-(phenylcarbamoyloxy)ethyl]amino]ethyl N-phenylcarbamate
State
State

At room temperature, Bambuterol is typically in a solid state. It is stable and does not sublimate or melt under normal conditions until it reaches its melting point.

Melting point (Celsius)
93.00
Melting point (Kelvin)
366.15
Boiling point (Celsius)
406.50
Boiling point (Kelvin)
679.65
General information
Molecular weight
521.66g/mol
Molar mass
521.6630g/mol
Density
1.2000g/cm3
Appearence

Bambuterol typically appears as a white to off-white crystalline powder. It is odorless and is usually provided in a pure, dry form for pharmaceutical use.

Comment on solubility

Solubility of 2-[2-(2-ethoxy-3-methoxy-phenyl)ethyl-[2-(phenylcarbamoyloxy)ethyl]amino]ethyl N-phenylcarbamate

Understanding the solubility of 2-[2-(2-ethoxy-3-methoxy-phenyl)ethyl-[2-(phenylcarbamoyloxy)ethyl]amino]ethyl N-phenylcarbamate is crucial for its application in various chemical processes. Solubility can vary widely based on several factors:

  • Polarity: The presence of polar functional groups often enhances solubility in polar solvents.
  • Hydrogen bonding: The potential for hydrogen bond formation can significantly affect solubility in protic solvents.
  • Temperature: As a general trend, solubility may increase with temperature, but specific behaviors can differ among compounds.
  • pH levels: The ionization of certain functional groups can change with pH, impacting solubility in aqueous environments.

It is essential to consider these factors when evaluating the solubility of this compound. In practical terms, while information on its exact solubility is limited, it is likely that the presence of ethoxy and methoxy groups enhances solubility in organic solvents, while its carbamate structure might provide solubility advantages in certain aqueous conditions. In summary, solubility is a multifaceted property that can greatly influence the behavior and utility of chemical compounds.

Interesting facts

Interesting Facts About 2-[2-(2-ethoxy-3-methoxy-phenyl)ethyl-[2-(phenylcarbamoyloxy)ethyl]amino]ethyl N-phenylcarbamate

This compound, although complex in its structure, offers a fascinating insight into the world of organic chemistry and medicinal applications. Here are some intriguing aspects of this unique molecule:

  • Functional Diversity: The compound contains multiple functional groups, including ethoxy, methoxy, and carbamate moieties, allowing for a variety of chemical interactions. This variety contributes to its potential biological activities.
  • Medicinal Relevance: Compounds like this one are often studied for their properties in drug design and development. The presence of the carbamate group can be significant in enhancing pharmacological activity and bioavailability.
  • Structure-Activity Relationship: Understanding the relationship between its molecular structure and biological effects is crucial. Each substituent on the aromatic rings can dramatically influence how the compound interacts with biological targets.
  • Synthetic Pathways: The synthesis of such complex compounds typically involves multiple steps of organic reactions, showcasing the ingenuity and precision in modern organic synthesis techniques.
  • Research Potential: Compounds with intricate structures can lead to new discoveries in medicinal chemistry, particularly in areas such as cancer treatment, where similar structures show promising antitumor activities.

As a chemistry student or researcher, exploring compounds like this can deepen your understanding of structure-function relationships and the intricate dance of atoms within a molecule. The ability to manipulate such compounds opens the door to innovative therapeutic solutions in pharmacology that can address unmet medical needs.

In summary, 2-[2-(2-ethoxy-3-methoxy-phenyl)ethyl-[2-(phenylcarbamoyloxy)ethyl]amino]ethyl N-phenylcarbamate stands out as a key example of how chemistry intersects with biology to potentially create the next wave of therapeutic agents.