Chlorphenesin carbamate
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- Molecular formula
- C11H15ClNO2
- CAS Number
- 104-29-0
- IUPAC Name
- 1-(4-chlorophenyl)-4-(dimethylamino)-2,3-dimethyl-butan-2-ol
- Molecular Weight
- 255.74g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2170g/cm3
- Synonyms
- Clobutinol
Identification
Interesting facts
Interesting Facts about 1-(4-chlorophenyl)-4-(dimethylamino)-2,3-dimethyl-butan-2-ol
1-(4-chlorophenyl)-4-(dimethylamino)-2,3-dimethyl-butan-2-ol is a fascinating compound that has drawn attention in various fields such as organic chemistry and medicinal applications. Here are some intriguing points regarding this compound:
- Pharmacological Interest: This compound, known for its unique structure, has potential pharmacological activities, particularly as an intermediate in the synthesis of various pharmaceuticals. Its functional groups make it a versatile building block in drug discovery.
- Chirality: The compound possesses chirality due to the presence of a stereocenter. This characteristic is vital, as it can lead to differences in biological activity between its enantiomers, making it an excellent candidate for chiral synthesis studies.
- Role in Organic Synthesis: The presence of the dimethylamino group enhances nucleophilicity, making this compound a useful reagent in various organic transformations, such as alkylation and acylation reactions.
- Potential Applications: Targeted research is being conducted to explore the applicability of this compound in synthesizing compounds with altered pharmacokinetics and pharmacodynamics, which can lead to new therapeutic agents.
- Electrophilic Substitution: The chlorophenyl moiety in the compound can serve as a site for electrophilic substitution reactions, paving the way for further functionalization and diversification of the compound's structure.
This compound exemplifies the complexity and potential of organic chemicals in modern chemistry. Its varied applications and fascinating structural attributes make it a subject of ongoing research and interest in the scientific community.