CAS 13080-86-9 2,2-Bis[4-(4-aminophenoxy)phenyl]propane

NAVIGATION

2,2-Bis[4-(4-aminophenoxy)phenyl]propane

PRICE INQUIRY

Catalog Number

ACM13080869-2

CAS Number

13080-86-9

Product Name

2,2-Bis[4-(4-aminophenoxy)phenyl]propane

Category

Monomers; Polymers

IUPAC Name

4-[4-[2-[4-(4-aminophenoxy)phenyl]propan-2-yl]phenoxy]aniline

Molecular Weight

410.5g/mol

Molecular Formula

C27H26N2O2

Canonical SMILES

CC(C)(C1=CC=C(C=C1)OC2=CC=C(C=C2)N)C3=CC=C(C=C3)OC4=CC=C(C=C4)N

InChI

InChI=1S/C27H26N2O2/c1-27(2,19-3-11-23(12-4-19)30-25-15-7-21(28)8-16-25)20-5-13-24(14-6-20)31-26-17-9-22(29)10-18-26/h3-18H,28-29H2,1-2H3

InChI Key

KMKWGXGSGPYISJ-UHFFFAOYSA-N

Application

2,2-Bis[4-(4-aminophenoxy)phenyl]propane (BAPP) is primarily utilized as a diamino monomer to facilitate the synthesis of advanced polymeric materials such as polyimides and epoxy resins. It features a distinctive diphenoxy-phenyl core with amine groups at both ends, which allows it to cross-link with carboxylic acids or dianhydrides. This ability makes it an invaluable component in producing polyimides that are employed in various applications including batteries, fuel cells, low dielectric materials, and OLEDs. BAPP contributes to creating polyimides with a glass transition temperature ranging from 225-230°C and demonstrates typical thermoplastic yield behavior, setting it apart from other polyimides. Additionally, BAPP serves an essential role in curing epoxy resins and poly(?-caprolactone) (PCL) to form crystalline thermoset blends, and is also used in developing dental resin composites, showcasing its versatility and importance in modern material science and engineering.

Complexity

475

Covalently-Bonded Unit Count

EC Number

235-985-8

Exact Mass

410.199428g/mol

Formal Charge

Heavy Atom Count

Monoisotopic Mass

410.199428g/mol

Rotatable Bond Count