2915-83-5

Basic information

• Product Name: 2,7-diamino-9H-fluoren-9-ol
• CAS NO: 2915-83-5
• Molecular Formula: C₁₃H₁₂N₂O
• Molecular Weight: 212.2472
• Mol File: 2915-83-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 521°C at 760 mmHg
• Flash Point: 268.9°C
• Density: 1.416g/cm³
• Vapor Pressure: 1.11E-11mmHg at 25°C
• Refractive Index: 1.796
• CAS DataBase Reference: 2,7-diamino-9H-fluoren-9-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,7-diamino-9H-fluoren-9-ol(2915-83-5)
• EPA Substance Registry System: 2,7-diamino-9H-fluoren-9-ol(2915-83-5)

Safety Data

• Hazardous Substances Data: 2915-83-5(Hazardous Substances Data)

Usage

Chemical class

Amines and phenols

Physical state

Solid at room temperature

Solubility

Insoluble in water, soluble in organic solvents

Applications

Organic synthesis, pharmaceuticals

Uses

Building block in the synthesis of organic molecules and pharmaceutical compounds

Biological activities

Antioxidant, anticancer properties

Upstream product

• 31551-45-8 2,7-dinitro-9-fluorenone 
• 2915-84-6 2,7-diaminofluoren-9-one 

Relevant articles and documents

A supramolecular sorting hat: Stereocontrol in metal-ligand self-assembly by complementary hydrogen bonding

A combination of self-complementary hydrogen bonding and metal-ligand interactions allows stereocontrol in the self-assembly of prochiral ligand scaffolds. A unique, non-tetrahedral M4L6 structure is observed upon multicomponent self-assembly of 2,7-diaminofluorenol with 2-formylpyridine and Fe(ClO4)2. The stereochemical outcome of the assembly is controlled by self-complementary hydrogen bonding between both individual ligands and a suitably sized counterion as template. This hydrogen-bonding-mediated stereoselective metal-ligand assembly allows the controlled formation of nonsymmetric discrete cage structures from previously unexploited ligand scaffolds. Abracadabra: The stereoselective self-assembly of an unsymmetrical metal-ligand cage can be controlled by self-complementary hydrogen bonding between alcohol-containing ligands as well as between ligands and suitable anion guests.