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CAS 163229-48-9

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1-(1,1-Dimethylethyl) 2-methyl 1H-indole-1,2-dicarboxylate

Description:
1-(1,1-Dimethylethyl) 2-methyl 1H-indole-1,2-dicarboxylate, with CAS number 163229-48-9, is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features two carboxylate groups, which contribute to its potential reactivity and solubility properties. The presence of the tert-butyl group (1,1-dimethylethyl) and a methyl group enhances its hydrophobic characteristics, influencing its interaction with biological systems and solvents. The indole moiety is known for its biological significance, often found in various natural products and pharmaceuticals. This compound may exhibit interesting pharmacological activities, making it a subject of interest in medicinal chemistry. Its synthesis and characterization would typically involve standard organic reactions, and its stability can be influenced by environmental factors such as temperature and pH. Overall, this compound's unique structure and functional groups suggest potential applications in drug development and other chemical research fields.
Formula:C15H17NO4
InChI:InChI=1S/C15H17NO4/c1-15(2,3)20-14(18)16-11-8-6-5-7-10(11)9-12(16)13(17)19-4/h5-9H,1-4H3
InChI key:InChIKey=UJVYYFYNECMKRA-UHFFFAOYSA-N
SMILES:C(OC(C)(C)C)(=O)N1C=2C(C=C1C(OC)=O)=CC=CC2
Synonyms:
  • 1-(1,1-Dimethylethyl) 2-methyl 1H-indole-1,2-dicarboxylate
  • 1-(tert-Butyl)-2-methyl-1H-indole-1,2-dicarboxylate 97%
  • 1H-Indole-1,2-dicarboxylic acid, 1-(1,1-dimethylethyl) 2-methyl ester
  • Boc-Methyl Indole-2-Carboxylate
  • Methyl N-Boc-indole-2-carboxylate
  • Methyl indole-2-carboxylate, N-BOC protected
  • Methyl indole-2-carboxylate, N-BOC protected 97%
  • 1-(tert-Butyl) 2-methyl 1H-indole-1,2-dicarboxylate
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