2,2-Bis(4-cyanatophenyl)propane

CAS: 1156-51-0

Ref. 3D-FB33798

Información del producto

• Nombre: 2,2-Bis(4-cyanatophenyl)propane
• Sinónimos: 2,2-Propanediyldi-4,1-phenylenedicyanate 4-(1-(4-(Cyanooxy)phenyl)-1-methylethyl)phenylcyanate, 2,2-Bis(p-cyanatophenyl)propane, 4,4′-Dicyanatodiphenyldimethylmethane, 4,4′-Isopropylidene diphenylcyanate, 4,4′-Isopropylidenediphenyl dicyanate, AroCy B 10, AroCy B 40, AroCy B 40S, B 40S, Ba 3000, Badcy, Bandy, BisCPP, Bisphenol A Dicyanate, Bisphenol A cyanate, Bisphenol A cyanate ester, CX (cyanate ester), Ca 210, Ce 01Mo, Cyanic acid, (1-methylethylidene)di-4,1-phenylene ester, Cyanic acid, C,C′-[(1-methylethylidene)di-4,1-phenylene] ester, Cyanic acid, isopropylidenedi-p-phenylene ester, Cytester TA, Dian dicyanate, Dicyanatobisphenol A, HF 1 (cyanate ester), Hf 10, Isopropylidenedi-p-phenylene cyanate, Ku 6537, Lonza BADCY, NSC 646242, Primaset BA 3000, Primaset BADCY, Propane-2,2-Diyldibenzene-4,1-Diyl Dicyanate, Skylex CA 200, Skylex CA 260, Ta 1500
• CAS: 1156-51-0

Descripción

2,2-Bis(4-cyanatophenyl)propane is a chemical species that belongs to the group of cyanates. It is a colorless liquid with a sweet odor and is highly soluble in water. 2,2-Bis(4-cyanatophenyl)propane has been shown to inhibit the formation of bisphenol A by reacting with the hydroxyl groups on the aromatic ring. The reaction mechanism may involve an oxidation process followed by nucleophilic substitution or addition. Zirconium oxide has been shown to activate 2,2-bis(4-cyanatophenyl)propane when heated at high temperatures, which leads to an increase in its kinetic data in a gravimetric analysis. This activation may be due to thermal expansion, leading to changes in the electronic structure of zirconium oxide and an increase in its electron affinity.

• Marca: Biosynth

Propiedades químicas

• Peso molecular: 278.31 g/mol
• Fórmula: C₁₇H₁₄N₂O₂
• Pureza: Min. 98 Area-%
• Color/Forma: White Powder
• SMILES: CC(C)(c1ccc(OC#N)cc1)c1ccc(OC#N)cc1