38557-26-5

Basic information

• Product Name: Benzonitrile, 2,6-bis(4-aminophenoxy)-
• CAS NO: 38557-26-5
• Molecular Formula: C19H15N3O2
• Molecular Weight: 317.347
• Mol File: 38557-26-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzonitrile, 2,6-bis(4-aminophenoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzonitrile, 2,6-bis(4-aminophenoxy)-(38557-26-5)
• EPA Substance Registry System: Benzonitrile, 2,6-bis(4-aminophenoxy)-(38557-26-5)

Safety Data

• Hazardous Substances Data: 38557-26-5(Hazardous Substances Data)

Upstream product

• 123-30-8 4-amino-phenol 
• 97027-19-5 2-chloro-6-(4-aminophenoxy)benzonitrile 
• 591-27-5 m-Hydroxyaniline 
• 1194-65-6 2,6-dichloro-benzonitrile 

Relevant articles and documents

Poly(amide imide)s containing functional nitrile groups for high performance materials

Novel poly(amide imide)s containing functional nitrile groups were prepared by one step polycondensation reaction of two new diacid chlorides having nitrile substituents with various aromatic diamines incorporating flexible ether bridges. The polymers wer

Synthesis and characterization of unsymmetrical benzonitrile-containing polyimides: Viscosity-lowering effect and dielectric properties

A new unsymmetrical diamine, 2-(3-aminophenoxy)-6-(4-aminophenoxy) benzonitrile (3,4-APBN), is synthesized via two consecutive SNAr reactions and the temperature-dependent reactivity of the fluorides in 2,6-difluorobenzonitrile, whose first SNAr reaction occurs at 70 °C and second, at 100 °C, allowing timing control of reaction sequence and circumventing the transetherification side reaction. Thus, a series of polyimides (PIs) is prepared from the polymerization of 3,4-APBN with five common dianhydrides (6FDA, DSDA, OPDA, BTDA, and PMDA). For comparison, a second series is also prepared from two symmetrical diamines ([2,6-bis(3-aminophenoxy) benzonitrile (3,3-APBN) and 2,6-bis(4-aminophenoxy)benzonitrile (4,4-APBN)] and 6FDA or PMDA. The processability of the poly(amic acids) (PAAs), for the first series is greatly improved since their solution viscosities are much lower than PAAs based on symmetrical diamines. Besides having high glass-transition temperatures (249-332 °C), and thermal stability [5% weight loss in the range of 505-542 °C (air) and 512-546 °C (nitrogen)], these PIs form tough, transparent and flexible films that have a tensile-strength range of 82.1-121.3 MPa, elongations-at-break of 5.33-9.81%, and tensile moduli of 2.11-2.97 GPa. Their film dielectric constants are 3.08-3.62 at 10 kHz, moderately higher than that (2.92) of analogous PI (CP2) without nitrile groups. Overall, we found that the reduction of structural symmetry in repeat units can improve the polymer processibility as well as increasing their dielectric constants. Copyright

New polyimides containing siloxane groups in the main chain

A series of polyimides and intermediate polyamidic acids has been synthesized by solution polycondensation reaction at high temperature of aromatic diamines containing flexible hexafluoroisopropylidene groups or cyano substituents with a dianhydride conta