6078-02-0

Basic information

• Product Name: Phenol, 2-[(2-furanylmethylene)amino]-
• CAS NO: 6078-02-0
• Molecular Formula: C11H9NO2
• Molecular Weight: 187.198
• Mol File: 6078-02-0.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: Phenol, 2-[(2-furanylmethylene)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-[(2-furanylmethylene)amino]-(6078-02-0)
• EPA Substance Registry System: Phenol, 2-[(2-furanylmethylene)amino]-(6078-02-0)

Safety Data

• Hazardous Substances Data: 6078-02-0(Hazardous Substances Data)

Upstream product

• 98-01-1 furfural 
• 95-55-6 2-amino-phenol 

Downstream Products

• 881-60-7 2-(furan-2-yl)benzoxazole 
• 59256-46-1 (2Z)-4-[(2-hydroxyphenyl)amino]-4-oxobut-2-enoic acid 

Relevant articles and documents

Novel R3M (M = Si, Ge) substituted furan and thiophene-derived aldimines: Synthesis, electrochemistry, and biological activity

New furan and thiophene derivatives of aldimines o-HO-C6H4N[dbnd]CHC4H4X(R) (X = O, S; R = H, SiMe3, SiEt3, GeMe3, GeEt3) were synthesized by condensation of o-aminoph

N,O-Amino-phenolate Mg(II) and Zn(II) Schiff base complexes: Synthesis and application in ring-opening polymerization of ε-caprolactone and lactides

Solventless grinding of 2-aminophenol and the corresponding aldehyde furnished compounds 2-(pyridin-2-ylmethylene)aminophenol (L1), 2-(pyridin-4-ylmethylene)aminophenol (L2), 2-(thiophen-2-ylmethylene)aminophenol (L3) and 2-(furan-2-ylmethylene)aminopheno

Enantioselective Strecker and Allylation Reactions with Aldimines Catalyzed by Chiral Oxazaborolidinium Ions

Chiral oxazaborolidinium ion (COBI)-catalyzed enantioselective nucleophilic addition reactions of aldimines using tributyltin cyanide and allyltributylstannane have been developed. Various α-aminonitriles and homoallylic amines were synthesized in high yi