132906-25-3

Basic information

• Product Name: Indole, derivative of
• Synonyms: Indole, derivative of
• CAS NO: 132906-25-3
• Molecular Formula: C₁₁H₁₂N₂O
• Molecular Weight: 236.26858
• Mol File: 132906-25-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Indole, derivative of(CAS DataBase Reference)
• NIST Chemistry Reference: Indole, derivative of(132906-25-3)
• EPA Substance Registry System: Indole, derivative of(132906-25-3)

Safety Data

• Hazardous Substances Data: 132906-25-3(Hazardous Substances Data)

Upstream product

• 1912-33-0 Indole-3-acetic acid methyl ester 
• 74-89-5 methylamine 
• 885117-59-9 methyl 3-(2-(methylamino)-2-oxoethyl)-1H-indole-1-carboxylate 
• 778-82-5 ethyl 3-indoleacetate 
• 87-51-4 indole-3-acetic acid 
• 879-37-8 3-indolylacetamide 
• 74-88-4 methyl iodide 

Downstream Products

• 1383933-74-1 (3aS,8aR)-1-methyl-3a-phenyl-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-2(1H)-one 

Relevant articles and documents

Reactions of the cyclic tautomer of 3-indoleacetamides. Synthesis of N(b)-methyl-4,5,6-tribromo-3-indoleacetamide

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Enantioselective copper-catalyzed construction of aryl pyrroloindolines via an arylation-cyclization cascade

An enantioselective arylation-cyclization cascade has been accomplished using a combination of diaryliodonium salts and asymmetric copper catalysis. These mild catalytic conditions provide a new strategy for the enantioselective construction of pyrroloindolines, an important alkaloid structural motif that is commonly found among biologically active natural products.

Synthesis of indolylmaleimides

The present invention provides a method for synthesizing indolylmaleimides by reacting an activated maleimide preferably with an optionally substituted organometallic-3-indole in the presence of a transition metal catalyst.