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CAS 1286273-59-3

:

1,1-Dimethylethyl N-[trans-4-[[(4-bromophenyl)methyl]amino]cyclohexyl]carbamate

Description:
1,1-Dimethylethyl N-[trans-4-[[(4-bromophenyl)methyl]amino]cyclohexyl]carbamate, identified by its CAS number 1286273-59-3, is a chemical compound characterized by its complex structure, which includes a carbamate functional group. This compound features a tert-butyl group, which contributes to its steric hindrance, and a cyclohexyl ring that enhances its hydrophobic properties. The presence of a bromophenyl moiety suggests potential for significant biological activity, possibly influencing its interactions with biological targets. The trans configuration of the cyclohexyl substituent may affect the compound's conformational stability and reactivity. Additionally, the amino group indicates potential for hydrogen bonding, which could play a role in solubility and interaction with other molecules. Overall, this compound's unique structural features may contribute to its potential applications in pharmaceuticals or agrochemicals, although specific biological activity and toxicity profiles would require further investigation.
Formula:C18H27BrN2O2
InChI:InChI=1/C18H27BrN2O2/c1-18(2,3)23-17(22)21-16-10-8-15(9-11-16)20-12-13-4-6-14(19)7-5-13/h4-7,15-16,20H,8-12H2,1-3H3,(H,21,22)/t15-,16-
InChI key:InChIKey=LZNQEZBYVGBLEX-WKILWMFINA-N
SMILES:N(C(OC(C)(C)C)=O)[C@H]1CC[C@H](NCC2=CC=C(Br)C=C2)CC1
Synonyms:
  • Carbamic acid, N-[trans-4-[[(4-bromophenyl)methyl]amino]cyclohexyl]-, 1,1-dimethylethyl ester
  • 1,1-Dimethylethyl N-[trans-4-[[(4-bromophenyl)methyl]amino]cyclohexyl]carbamate
  • TERT-BUTYL (TRANS-4-((4-BROMOBENZYL)AMINO)CYCLOHEXYL)CARBAMATE
  • tert-Butyl (1R*,4R*)-4-(4-bromobenzylamino)cyclohexylcarbamate
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