332056-10-7

Basic information

• Product Name: 3-amino-1-(3-methoxyphenyl)-1H-benzo[f]chromene-2-carbonitrile
• Synonyms: 3-amino-1-(3-methoxyphenyl)-1H-benzo[f]chromene-2-carbonitrile
• CAS NO: 332056-10-7
• Molecular Formula: C₂₁H₁₆N₂O₂
• Molecular Weight: 328.36394
• Mol File: 332056-10-7.mol
• Article Data: 14

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-amino-1-(3-methoxyphenyl)-1H-benzo[f]chromene-2-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 3-amino-1-(3-methoxyphenyl)-1H-benzo[f]chromene-2-carbonitrile(332056-10-7)
• EPA Substance Registry System: 3-amino-1-(3-methoxyphenyl)-1H-benzo[f]chromene-2-carbonitrile(332056-10-7)

Safety Data

• Hazardous Substances Data: 332056-10-7(Hazardous Substances Data)

Upstream product

• 591-31-1 3-methoxy-benzaldehyde 
• 2972-72-7 2-(3-methoxybenzylidene)malononitrile 
• 135-19-3 β-naphthol 
• 109-77-3 malononitrile 
• 90-15-3 α-naphthol 

Downstream Products

• 1621314-70-2 9-chloromethyl-12-(m-methoxyphenyl)-10,12-dihydrobenzo[5,6]chromeno[2,3-d]pyrimidin-11-one 
• 1621314-54-2 2-chloro-N-(2-cyano-1-(m-methoxyphenyl)-1H-benzo[f]chromen-3-yl)acetamide 
• 1300713-42-1 14-(3'-methoxyphenyl)-10,11,12,14-tetrahydro-9H-benzo[5,6]chromeno[2,3-b]quinolin-13-amine 

Relevant articles and documents

Bipyridinium chloride supported rice husk silica: An efficient nanocomposite for the one-pot preparation of spirooxindole pyran and 2-amino-4h-chromene derivatives

In this paper, rice-husk-silica supported n-propyl bipyridinium chloride (RHPrBPCl) has been prepared as a heterogeneous catalyst. RHPrBPCl has been successfully applied in the one-pot preparation of spirooxindole pyran and 2-amino- 4H-chromene derivative

One-pot Synthesis of 2-Amino-4H-Chromenes using Chicken Eggshell Waste as Green Catalyst under Solvent-Free Conditions

Chicken eggshell waste has been employed as green and efficient catalyst for the preparation of 2-amino-4H-chromenes. The aromatic aldehydes were condensed with malononitrile and 1-naphthol or 2-naphthol under solvent-free condition in the presence of chi

Triethanolamine-catalyzed expeditious and greener synthesis of 2-amino-4H-chromenes

Triethanolamine (TEOA), an inexpensive and eco-friendly base, was used to efficiently catalyze the three-component condensation reaction of heterocyclic/aromatic aldehyde, (α/β)-naphthol, and malononitrile in water to give the corresponding substituted 2-