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CAS 1123169-45-8

:

1,1-Dimethylethyl 6-bromo-3,4-dihydro-1(2H)-quinolinecarboxylate

Description:
1,1-Dimethylethyl 6-bromo-3,4-dihydro-1(2H)-quinolinecarboxylate, with the CAS number 1123169-45-8, is a chemical compound characterized by its unique structure that includes a quinoline moiety, a bromine atom, and an ester functional group. This compound typically exhibits properties associated with both the quinoline and ester functionalities, such as potential biological activity and solubility in organic solvents. The presence of the bromine atom may impart specific reactivity and influence the compound's pharmacological properties. Additionally, the dimethyl group contributes to steric hindrance, which can affect the compound's interactions with biological targets. As a derivative of quinoline, it may exhibit various activities, including antimicrobial or anticancer properties, making it of interest in medicinal chemistry. However, detailed studies would be necessary to fully elucidate its properties, reactivity, and potential applications in pharmaceuticals or other fields. Safety and handling precautions should be observed due to the presence of bromine and the potential for biological activity.
Formula:C14H18BrNO2
InChI:InChI=1S/C14H18BrNO2/c1-14(2,3)18-13(17)16-8-4-5-10-9-11(15)6-7-12(10)16/h6-7,9H,4-5,8H2,1-3H3
InChI key:InChIKey=HXVKARGTRMNFQU-UHFFFAOYSA-N
SMILES:C(OC(C)(C)C)(=O)N1C=2C(CCC1)=CC(Br)=CC2
Synonyms:
  • tert-Butyl 6-bromo-3,4-dihydroquinoline-1(2H)-carboxylate
  • 1,1-Dimethylethyl 6-bromo-3,4-dihydro-1(2H)-quinolinecarboxylate
  • 1(2H)-Quinolinecarboxylic acid, 6-bromo-3,4-dihydro-, 1,1-dimethylethyl ester
  • tert-Butyl 6-bromo-3,4-dihydro-2H-quinoline-1-carboxylate
  • 6-Bromo-1,2,3,4-tetrahydroquinoline-1-carboxylic acid tert-butyl ester
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