Interesting facts
Interesting Facts About Ethyl N-benzyl-N-cyclopropyl-carbamate
Ethyl N-benzyl-N-cyclopropyl-carbamate is a fascinating compound that belongs to the class of carbamates, which are known for their diverse applications in both biological and industrial contexts. Here are some intriguing points about this compound:
- Pharmaceutical Applications: Carbamates, including ethyl N-benzyl-N-cyclopropyl-carbamate, play a significant role in medicinal chemistry. They often exhibit activities such as antidepressant and antimicrobial properties, making them important in drug development.
- Unique Structure: The presence of the cyclopropyl group adds a distinctive twist to the molecular architecture, often influencing the compound's reactivity and interaction with biological targets.
- Source of Inspiration: Chemists often draw inspiration from naturally occurring structures when designing carbamate derivatives. Understanding how modifications like benzyl and cyclopropyl groups affect biological activity can lead to the discovery of new therapeutic agents.
- Regulatory Considerations: When considering the synthesis and application of carbamates, understanding environmental impact is crucial. Some carbamates may exhibit toxicity to non-target organisms, hence requiring careful evaluations and regulatory measures.
- Synthesis Techniques: Chemists utilize various methods to synthesize ethyl N-benzyl-N-cyclopropyl-carbamate, including nucleophilic substitution reactions and carbamic acid derivatives. The choice of method often depends on desired yield and purity.
In summary, ethyl N-benzyl-N-cyclopropyl-carbamate illustrates the intricate balance between chemistry, biology, and environmental stewardship. Its unique features and broad applications continue to intrigue scientists venturing into the realms of drug discovery and synthetic chemistry.
Synonyms
Encyprate
2521-01-9
Ethyl N-benzyl-N-cyclopropylcarbamate
Enciprato
Ethyl N-benzylcyclopropanecarbamate
MO-1255
Encypratum [Latin]
Carbamic acid, cyclopropyl(phenylmethyl)-, ethyl ester
Enciprato [Spanish]
A-19757
Encypratum
Encyprate [USAN:INN]
Encypratum [INN-Latin]
Enciprato [INN-Spanish]
NSC 43799
NSC-43799
NSC 169504
NSC-169504
A 19757
26991ZCA4G
ENCYPRATE [INN]
ENCYPRATE [USAN]
BRN 2648343
CYCLOPROPANECARBAMIC ACID, N-BENZYL-, ETHYL ESTER
DTXSID90179870
Encypratum (Latin)
Encypratum (INN-Latin)
Enciprato (INN-Spanish)
DTXCID50102361
684-194-8
MLS002608573
N-Carbethoxy-N-benzyl-cyclopropylamine
MO 1255
WLN: L3TJ AN1R&VO2
Cyclopropanecarbamic acid, ethyl ester
Encyprat
Encyprate (USAN/INN)
SCHEMBL122353
UNII-26991ZCA4G
CHEMBL2104204
Ethyl benzyl(cyclopropyl)carbamate
OGXBVBBMMWSZJO-UHFFFAOYSA-N
HMS3092J23
NSC43799
NSC169504
AKOS009148189
SMR001527320
NS00124034
D03993
Q27254078
Solubility of Ethyl N-benzyl-N-cyclopropyl-carbamate
Ethyl N-benzyl-N-cyclopropyl-carbamate, a compound with an interesting structure, exhibits specific solubility characteristics that are worth noting:
In summary, the solubility of ethyl N-benzyl-N-cyclopropyl-carbamate will typically align more closely with organic solvents, reflecting a tendency to exhibit greater solubility in non-polar environments while showing limited interaction with highly polar solvents. Therefore, when considering solubility profiles, one might echo the notion: "Like dissolves like."