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CAS 1228690-37-6

:

(1R)-1-Phenylethyl N-[5-(4-bromophenyl)-3-methyl-4-isoxazolyl]carbamate

Description:
(1R)-1-Phenylethyl N-[5-(4-bromophenyl)-3-methyl-4-isoxazolyl]carbamate is a chemical compound characterized by its complex structure, which includes a phenylethyl moiety and an isoxazole ring. The presence of the bromophenyl group suggests potential for significant biological activity, as halogenated aromatic compounds often exhibit unique interactions in biological systems. The carbamate functional group indicates that this compound may have applications in medicinal chemistry, potentially acting as an inhibitor or modulator in various biochemical pathways. Its stereochemistry, denoted by the (1R) configuration, implies that it may exhibit specific interactions with biological targets, which can be crucial for its efficacy and safety profile. The compound's solubility, stability, and reactivity would depend on its functional groups and overall molecular structure, influencing its potential applications in pharmaceuticals or agrochemicals. Further studies would be necessary to elucidate its precise biological activity and potential therapeutic uses.
Formula:C19H17BrN2O3
InChI:InChI=1S/C19H17BrN2O3/c1-12-17(18(25-22-12)15-8-10-16(20)11-9-15)21-19(23)24-13(2)14-6-4-3-5-7-14/h3-11,13H,1-2H3,(H,21,23)/t13-/m1/s1
InChI key:InChIKey=YIZLYJGOEIDGMD-CYBMUJFWSA-N
SMILES:N(C(O[C@H](C)C1=CC=CC=C1)=O)C2=C(ON=C2C)C3=CC=C(Br)C=C3
Synonyms:
  • Carbamic acid, N-[5-(4-bromophenyl)-3-methyl-4-isoxazolyl]-, (1R)-1-phenylethyl ester
  • [5-(4-Bromophenyl)-3-methylisoxazol-4-yl]carbamic acid (R)-1-phenylethyl ester
  • (1R)-1-Phenylethyl N-[5-(4-bromophenyl)-3-methyl-4-isoxazolyl]carbamate
  • (R)-1-Phenylethyl (5-(4-bromophenyl)-3-methylisoxazol-4-yl)carbamate
  • BMS-986020 INT
  • EOS-60370
  • 1-Phenylethyl (R)-[5-(4-Bromophenyl)-3-methyl-4-isoxazolyl]carbamate
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