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CAS 123387-53-1

:

1(2H)-Quinolinecarboxylic acid, 3,4-dihydro-, 1,1-dimethylethyl ester

Description:
1(2H)-Quinolinecarboxylic acid, 3,4-dihydro-, 1,1-dimethylethyl ester, also known by its CAS number 123387-53-1, is an organic compound characterized by its quinoline structure, which is a bicyclic aromatic compound. This substance features a carboxylic acid functional group that is esterified with a tert-butyl group, contributing to its hydrophobic properties. The presence of the dihydroquinoline moiety indicates that it has a saturated ring system, which can influence its reactivity and stability. Typically, compounds of this nature exhibit moderate to low solubility in water but are more soluble in organic solvents due to their hydrophobic characteristics. They may also display biological activity, making them of interest in medicinal chemistry and drug development. The compound's structure suggests potential applications in various fields, including pharmaceuticals and agrochemicals, although specific biological activities would require further investigation. Safety data and handling precautions should be considered, as with any chemical substance, to ensure proper laboratory practices.
Formula:C14H19NO2
InChI:InChI=1S/C14H19NO2/c1-14(2,3)17-13(16)15-10-6-8-11-7-4-5-9-12(11)15/h4-5,7,9H,6,8,10H2,1-3H3
InChI key:InChIKey=GVSRWAIRQCMAHG-UHFFFAOYSA-N
SMILES:C(OC(C)(C)C)(=O)N1C=2C(CCC1)=CC=CC2
Synonyms:
  • N-Boc-1,2,3,4-tetrahydroquinoline
  • tert-Butyl 3,4-dihydro-1(2H)-quinolinecarboxylate
  • 1,1-Dimethylethyl 3,4-dihydro-1(2H)-quinolinecarboxylate
  • 1(2H)-Quinolinecarboxylic acid, 3,4-dihydro-, 1,1-dimethylethyl ester
  • 1-BOC-1,2,3,4-Tetrahydroquinoline
  • tert-Butyl 3,4-dihydroquinoline-1(2H)-carboxylate
  • tert-butyl 1,2,3,4-tetrahydroquinoline-1-carboxylate
  • t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylate
  • tert-butyl 3,4-dihydro-2H-quinoline-1-carboxylate
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