1629243-84-0

Basic information

• Product Name: 2′-amino-6′-benzyl-1-butyl-2,5′-dioxo-1,2,6′,7′-tetrahydro-5′H-spiro[indole-3,4′-pyrano[2,3-c]pyrrole]-3′-carbonitrile
• Synonyms: 2′-amino-6′-benzyl-1-butyl-2,5′-dioxo-1,2,6′,7′-tetrahydro-5′H-spiro[indole-3,4′-pyrano[2,3-c]pyrrole]-3′-carbonitrile
• CAS NO: 1629243-84-0
• Molecular Weight: 440.502
• Mol File: 1629243-84-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2′-amino-6′-benzyl-1-butyl-2,5′-dioxo-1,2,6′,7′-tetrahydro-5′H-spiro[indole-3,4′-pyrano[2,3-c]pyrrole]-3′-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2′-amino-6′-benzyl-1-butyl-2,5′-dioxo-1,2,6′,7′-tetrahydro-5′H-spiro[indole-3,4′-pyrano[2,3-c]pyrrole]-3′-carbonitrile(1629243-84-0)
• EPA Substance Registry System: 2′-amino-6′-benzyl-1-butyl-2,5′-dioxo-1,2,6′,7′-tetrahydro-5′H-spiro[indole-3,4′-pyrano[2,3-c]pyrrole]-3′-carbonitrile(1629243-84-0)

Safety Data

• Hazardous Substances Data: 1629243-84-0(Hazardous Substances Data)

Upstream product

• 4290-91-9 N-butylisatin 
• 109-77-3 malononitrile 

Relevant articles and documents

Efficient catalyst-free one-pot three-component synthesis of novel spirooxindole derivatives, and their cytotoxic activities

A simple and efficient one-pot approach for assembling novel spiro[indolepyranopyrrole] derivatives was developed and used to prepare a series of biologically important compounds. The reaction was easily performed with high efficiency under very simple and mild conditions without any catalysts and it gave good yields, avoiding time-consuming costly synthesis and laborious workup and purification of products. The cytotoxic activities of these new spiro[indolepyranopyrrole] derivatives were evaluated in vitro. Most of the tested compounds exhibited significant cytotoxicities to Raji cell lines. Georg Thieme Verlag Stuttgart New York.