476479-85-3

Basic information

• Product Name: 6-Chloro-2-imino-2H-chromene-3-carbonitrile
• Synonyms: 6-Chloro-2-imino-2H-chromene-3-carbonitrile
• CAS NO: 476479-85-3
• Molecular Weight: 204.615
• Mol File: 476479-85-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-Chloro-2-imino-2H-chromene-3-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Chloro-2-imino-2H-chromene-3-carbonitrile(476479-85-3)
• EPA Substance Registry System: 6-Chloro-2-imino-2H-chromene-3-carbonitrile(476479-85-3)

Safety Data

• Hazardous Substances Data: 476479-85-3(Hazardous Substances Data)

Upstream product

• 2420-26-0 4-chlorosalicylaldehyde 
• 109-77-3 malononitrile 

Downstream Products

• 175136-95-5 2(-2-amino-6-chloro-3-cyano-4H-chromen-4-yl)malononitrile 
• 28447-81-6 6-chloro-2-oxo-2H-chromene-3-carbonitrile 
• 1430822-94-8 4-chloro-2-(7-chloro-(4-diethylamino)-5H-chromeno[2,3-d]pyrimidin-2-yl)phenol 
• 1430822-91-5 4-chloro-2-(7-chloro-(4-dimethylamino)-5H-chromeno[2,3-d]pyrimidin-2-yl)phenol 

Relevant articles and documents

Copper-Catalyzed Imino C-N Bond Formation with Aryl Boronic Acids under Aerobic Conditions

A copper-catalyzed, ligand- and base-free C-N cross-coupling reaction of iminochromenes with arylboronic acids in a nontoxic ethanol solvent at room temperature under air is developed. The product yields are found to be good to moderate. The conservation of the sensitive imine functional group implies the mildness of this protocol.