2,2-Bis(4-aminophenyl)hexafluoropropane

CAS : 1095-78-9

Ref. 3D-FB62708

Informations sur le produit

• Nom: 2,2-Bis(4-aminophenyl)hexafluoropropane
• Synonymes: 4,4'-(Hexafluoroisopropylidene)dianiline, 2,2-Bis(4-aminophenyl)-1,1,1,3,3,3-hexafluoropropane, 2-Bromo-6-chloro-4-(trifluoromethyl)aniline, 4,4'-(1,1,1,3,3,3-Hexafluoropropane-2,2-Diyl)Dibenzene-1,2-Diamine, 4,4′-(Hexafluoroisopropylidene)dianiline, 4,4′-[2,2,2-Trifluoro-1-(trifluoromethyl)ethylidene]bis[benzenamine], Aniline, 4,4′-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]di-, Aniline, 4,4′-[trifluoro-1-(trifluoromethyl)ethylidene]di-, Benzenamine, 2-bromo-6-chloro-4-(trifluoromethyl)-, Benzenamine, 4,4′-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-, Bis-A-Af, Hexafluoroisopropylidene-4,4′-dianiline
• CAS: 1095-78-9

Description

2,2-Bis(4-aminophenyl)hexafluoropropane (BPAP) is a monomer that can be used to synthesize polymers with a variety of properties. It has high potential use in the field of gas separation due to its ability to separate gases by size. BPAP is soluble in water and hydrochloric acid, and reacts with hydroxide solution and chloride to form hydrogen fluoride. This monomer has a molecular weight of 156 Da. It is synthesized from the reaction between 4-aminobenzoic acid and hexafluoroacetone. The molecular modelling shows that the molecule has six different conformations, with each conformation possessing a different shape. It also displays a certain amount of flexibility as it can bend or twist without breaking apart. BPAP is insoluble in organic solvents such as benzene or chloroform, but is soluble in hydrocarbons such as tetrahydrofuran or

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 334.26 g/mol
• Formule: C₁₅H₁₂F₆N₂
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C15H12F6N2/c16-14(17,18)13(15(19,20)21,9-1-5-11(22)6-2-9)10-3-7-12(23)8-4-10/h1-8H,22-23H2
• Code InChI: InChIKey=BEKFRNOZJSYWKZ-UHFFFAOYSA-N
• SMILES: Nc1ccc(C(c2ccc(N)cc2)(C(F)(F)F)C(F)(F)F)cc1