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CAS 1187386-06-6

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Phenylmethyl N-[1-(4-bromophenyl)cyclopropyl]carbamate

Description:
Phenylmethyl N-[1-(4-bromophenyl)cyclopropyl]carbamate is a chemical compound characterized by its unique structure, which includes a carbamate functional group linked to a cyclopropyl moiety and a bromophenyl substituent. This compound typically exhibits properties associated with both the carbamate and aromatic functionalities, such as potential biological activity and solubility in organic solvents. The presence of the bromine atom in the para position of the phenyl ring may influence its reactivity and interaction with biological targets, potentially enhancing its pharmacological properties. The cyclopropyl group can impart strain and unique steric effects, which may also affect the compound's overall behavior in chemical reactions or biological systems. As with many carbamates, it may exhibit moderate to high stability under standard conditions, but can be hydrolyzed in the presence of strong acids or bases. Overall, the characteristics of this compound suggest it may have applications in medicinal chemistry or as a research tool in studying specific biological pathways.
Formula:C17H16BrNO2
InChI:InChI=1S/C17H16BrNO2/c18-15-8-6-14(7-9-15)17(10-11-17)19-16(20)21-12-13-4-2-1-3-5-13/h1-9H,10-12H2,(H,19,20)
InChI key:InChIKey=JEQGBWWBXOGYMZ-UHFFFAOYSA-N
SMILES:N(C(OCC1=CC=CC=C1)=O)C2(CC2)C3=CC=C(Br)C=C3
Synonyms:
  • Benzyl [1-(4-bromophenyl)cyclopropyl]carbamate
  • Phenylmethyl N-[1-(4-bromophenyl)cyclopropyl]carbamate
  • Carbamic acid, N-[1-(4-bromophenyl)cyclopropyl]-, phenylmethyl ester
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