15419-92-8

Basic information

• Product Name: 1,2-Benzenediamine, N,N'-bis(2-furanylmethylene)-
• CAS NO: 15419-92-8
• Molecular Formula: C16H12N2O2
• Molecular Weight: 264.283
• Mol File: 15419-92-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,2-Benzenediamine, N,N'-bis(2-furanylmethylene)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzenediamine, N,N'-bis(2-furanylmethylene)-(15419-92-8)
• EPA Substance Registry System: 1,2-Benzenediamine, N,N'-bis(2-furanylmethylene)-(15419-92-8)

Safety Data

• Hazardous Substances Data: 15419-92-8(Hazardous Substances Data)

Usage

Structure

Benzene ring with two amino groups (-NH2) and two furan rings (C4H4O) attached to the amino groups.

Production of polymers and resins

Used as a building block or monomer in the synthesis of various polymers and resins.

Synthesis of organic compounds

Utilized as an intermediate in the synthesis of other organic compounds.

Potential skin irritant and sensitizer

Can cause skin irritation and allergic reactions upon contact.

Mutagenic properties

Has the potential to cause genetic mutations.

Carcinogenic properties

May have the ability to cause cancer.

Upstream product

• 98-01-1 furfural 
• 95-54-5 1,2-diamino-benzene 

Downstream Products

• 57490-73-0 2,3-di-furan-2-yl-quinoxaline 

Relevant articles and documents

Facile Synthesis of 1,2-Disubstituted Benzimidazoles Usingp-Toluenesulfonic Acid through Grinding Method

Abstract: An efficient synthetic method for the highly selective synthesis ofpharmacologically active 1,2-disubstituted benzimidazole derivatives fromo-phenylenediamine and various aromaticaldehydes catalyzed by p-toluenesulfonic acidthrough grinding unde

Synthesis, characterization and biological activity of some platinum(II) complexes with Schiff bases derived from salicylaldehyde, 2-furaldehyde and phenylenediamine

Four platinum(II) complexes of Schiff bases derived from salicylaldehyde and 2-furaldehyde with o- and p-phenylenediamine were reported and characterized based on their elemental analyses, IR and UV-vis spectroscopy and thermal analyses (TGA). The complex

Cobalt(II)-Catalyzed Conversion of Allylic Alcohols/Acetates to Allylic Amides in the Presence of Nitriles

Various secondary allylic alcohols or their acetates and tertiary allylic alcohols can be converted to the corresponding transposed allylic amides in the presence of a catalytic quantity of cobalt(II) chloride and acetic anhydride in acetonitrile.Tertiary alcohols undergo complete rearrangement whereas secondary ones afford a mixture of regioisomers.Moderate yields of amides are also obtained by reacting acrylonitrile with secondary alcohols in 1,2-dichloroethane.The presence of acetic anhydride or acetic acid is crucial to the formation of amides as the absence of the former affords no amides and the allylic alcohols are mainly recovered as regioisomeric mixtures.The regioselectivity during amide formation can be enhanced by using cobalt complexes 14-16 in acetic acid medium.Some preliminary studies indicate that these reactions are proceeding via an ?-allyl complex or tight ion pair rather than a sigmatropic rearrangement of acetamidate obtained in a Pinner reaction.