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Indole-7-carboxylic acid is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
Yuji Enomoto.; Yoshio Furutani.; Hiroshi Naganawa.; Masa Hamada.; Tomio Takeuchi.; Hamao Umezawa. Studies on the total synthesis of CC-1065: preparation of a synthetic simplified 3-carbamoyl-1,2-dihydro-3H-pyrrolo[3,2-e]indole dimer/trimer/tetramer (CDPI dimer/trimer/tetramer) and development of methodology for PDE-I dimer methyl ester formation. J. Org. Chem. 1987, 52 (8), 1521-1530.
Dale L. Boger.; Robert S. Coleman.; Benedict J. Invergo. Micellar system in copper-catalyzed hydroxylation of arylboronic acids: facile access to phenols. Chemical Communications. 2011, 47 (42), 11775-11777.
Hazard Statements: H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Precautionary Statements: P261-P280a-P305+P351+P338-P304+P340-P405-P501a
Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.