876710-04-2

Basic information

• Product Name: 2-amino-6-(hydroxymethyl)-4-(3-methylphenyl)-8-oxo-4,8-dihydropyrano[3,2-b]pyran-3-carbonitrile
• Synonyms: 2-amino-6-(hydroxymethyl)-4-(3-methylphenyl)-8-oxo-4,8-dihydropyrano[3,2-b]pyran-3-carbonitrile
• CAS NO: 876710-04-2
• Molecular Weight: 310.309
• Mol File: 876710-04-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-amino-6-(hydroxymethyl)-4-(3-methylphenyl)-8-oxo-4,8-dihydropyrano[3,2-b]pyran-3-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-6-(hydroxymethyl)-4-(3-methylphenyl)-8-oxo-4,8-dihydropyrano[3,2-b]pyran-3-carbonitrile(876710-04-2)
• EPA Substance Registry System: 2-amino-6-(hydroxymethyl)-4-(3-methylphenyl)-8-oxo-4,8-dihydropyrano[3,2-b]pyran-3-carbonitrile(876710-04-2)

Safety Data

• Hazardous Substances Data: 876710-04-2(Hazardous Substances Data)

Usage

Properties

1. Amino group
2. Hydroxymethyl group
3. Carbonitrile group
4. Pyrano pyran ring system
5. 3-methylphenyl group
6. Oxo group
7. Heterocyclic compound
8. Highly functionalized structure

Chemical compound

2-amino-6-(hydroxymethyl)-4-(3-methylphenyl)-8-oxo-4,8-dihydropyrano[3,2-b]pyran-3-carbonitrile

Structure

Complex

Potential uses

Medicinal chemistry, building block for synthesis of other complex molecules

Further investigation needed

Research and experimentation to determine specific properties and applications

Upstream product

• 501-30-4 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one 
• 620-23-5 m-tolyl aldehyde 
• 109-77-3 malononitrile 
• 15728-26-4 2-(3-methylbenzylidene)malononitrile 

Relevant articles and documents

Microwave-assisted, water-mediated Michael addition for synthesis of kojic acid derivatives

A highly efficient method is described for the synthesis of substituted kojic acid derivatives in the presence of water under microwave irradiation. This transformation represents an efficient way to synthesize kojic acid derivatives from simple starting

One-pot synthesis of 2-amino-4,8-dihydropyrano[3,2-b]pyranes and pyridopyrimidines under mild conditions

1,8-Diazabicyclo[5.4.0]undec-7-ene immobilized on silica (SB-DBU)Cl as a reusable and heterogeneous catalyst was applied for the one-pot, three-component synthesis of 2-amino-4,8-dihydropyrano[3,2-b]pyrane-3-carbonitriles and pyridopyrimidines, under solvent-free conditions. The reaction was carried out at room temperature, and pure products were obtained in high yields and short reaction times (3–7 min). This work introduced an environmentally benign procedure for the synthesis of these classes of biological active compounds.

Synthesis, characterization, and application of Cu2O and NiO nanoparticles supported on natural nanozeolite clinoptilolite as a heterogeneous catalyst for the synthesis of pyrano[3,2-b]pyrans and pyrano[3,2-c]pyridones

In this research, Cu2O and NiO nanoparticles supported on natural nanozeolite clinoptilolite (CP) was found to be a recoverable catalyst system for synthesis of pyrano-[3,2-c]pyridone and pyrano[3,2-b]pyran derivatives in aqueous media. The nan