Chlorambucil
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- Molecular formula
- C14H19Cl2N1O2
- CAS Number
- 305-03-3
- IUPAC Name
- isopropyl N-[4-[bis(2-chloroethyl)amino]phenyl]carbamate
- Molecular Weight
- 304.21g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3010g/cm3
- Synonyms
- 2045-44-5
Identification
Interesting facts
Interesting Facts about Isopropyl N-[4-[bis(2-chloroethyl)amino]phenyl]carbamate
Isopropyl N-[4-[bis(2-chloroethyl)amino]phenyl]carbamate is a fascinating compound with a variety of applications, particularly in pharmaceuticals and chemical research. Here are some noteworthy aspects:
- Pharmaceutical Relevance: This compound is often explored in the field of medicinal chemistry for its potential use as an anticancer agent. The presence of the bis(2-chloroethyl)amino group suggests that it may operate by alkylating DNA, a mechanism commonly utilized by chemotherapeutic agents.
- Structural Complexity: The structure includes a carbamate moiety, which is known for its ability to enhance the lipophilicity and bioavailability of drugs. This design allows for improved absorption and distribution within biological systems.
- Mechanism of Action: The bis(2-chloroethyl)amino group plays a critical role in the compound's mechanism of action. Its ability to form reactive intermediates capable of binding to DNA is crucial for inducing cell death in rapidly dividing cancer cells.
- Research Potential: Scientists are continuously investigating derivatives of this compound, aiming to optimize its effectiveness and reduce potential side effects. Structure-activity relationship (SAR) studies are key in this regard, helping researchers identify which modifications yield greater therapeutic benefits.
- Safety Considerations: As with many compounds featuring chloroethyl groups, careful consideration must be given to the toxicity and safety profiles of isopropyl N-[4-[bis(2-chloroethyl)amino]phenyl]carbamate. Ongoing research is essential to ensure that any therapeutic applications are both effective and safe for patients.
In summary, isopropyl N-[4-[bis(2-chloroethyl)amino]phenyl]carbamate stands out not only for its intricate molecular structure and potential as a therapeutic agent but also for the ongoing research that seeks to unlock its full capabilities in the fight against cancer.