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CAS 103733-31-9

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(S)-6,7-DIMETHOXY-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINE CARBOXYLIC TERT BUTYL ESTER

Description:
(S)-6,7-Dimethoxy-1,2,3,4-tetrahydro-3-isoquinoline carboxylic tert-butyl ester is a chemical compound characterized by its isoquinoline structure, which is a bicyclic compound featuring a fused benzene and pyridine ring. This specific compound is a chiral molecule, indicated by the (S) configuration, which refers to the spatial arrangement of its atoms. The presence of two methoxy groups (–OCH3) at the 6 and 7 positions enhances its solubility and reactivity. The tert-butyl ester functional group contributes to its stability and influences its pharmacokinetic properties, making it potentially useful in medicinal chemistry. The compound may exhibit biological activity, possibly related to its isoquinoline framework, which is known for various pharmacological effects. Its synthesis and characterization typically involve organic reactions that ensure the correct stereochemistry and functional group placement. As with many organic compounds, safety and handling precautions are essential due to potential toxicity or reactivity.
Formula:C16H23NO4
InChI:InChI=1/C16H23NO4/c1-16(2,3)21-15(18)12-6-10-7-13(19-4)14(20-5)8-11(10)9-17-12/h7-8,12,17H,6,9H2,1-5H3/t12-/m0/s1
SMILES:CC(C)(C)OC(=O)[C@@H]1Cc2cc(c(cc2CN1)OC)OC
Synonyms:
  • Tert-Butyl 6,7-Dimethoxy-1,2,3,4-Tetrahydroisoquinoline-3-Carboxylic Acid
  • tert-butyl (3S)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylate
  • (S)-1,2,3,4-Tetrahydro-6,7-diMethoxy-3-isoquinolinecarboxylic Acid 1,1-DiMethylethyl Ester
  • 3-Isoquinolinecarboxylic acid, 1,2,3,4-tetrahydro-6,7-dimethoxy-, 1,1-dimethylethyl ester, (S)- (9CI)
  • (S)-tert-Butyl 6,7-diMethoxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylate
  • Moexipril Impurity 16
  • (S)-6,7-DIMETHOXY-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINE CARBOXYLIC TERT BUTYL ESTER
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