4,4′-(Hexafluoroisopropylidene)bis(p-phenyleneoxy)dianiline (HFBAPP) - Moligand™,≥99% , K 2P10.1 activator; K 2P2.1 activator, CAS No.69563-88-8, K 2P10.1 activator; K 2P2.1 activator

CAS: 69563-88-8 Cat. No.: H1507157 Peso molecular: 518.45 Número EC: 626-703-8

GRADE & PURITY Moligand™, ≥99%

Storage

Room temperature

Shipped In

Normal

Specifications

Especificaciones y pureza

Moligand™, ≥99%

Mecanismos bioquímicos y fisiológicos

TREK1 and TREK2 channel activators (EC50=0.76 μ M in Rb efflux assay in CHO cells expressing TREK1). Compared with TRAAK, TASK3, and a series of other potassium ion channels, TREK1/2 exhibits selectivity. Hyperpolarized membrane potential of dorsal root g

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Grado

Moligand™

Tipo de acción

ACTIVATOR

Mecanismo de acción

K 2P10.1 activator; K 2P2.1 activator

Pureza

≥99%

Nombres e identificadores

• Sonrisas canónicas: NC1=CC=C(OC2=CC=C(C=C2)C(C2=CC=C(OC3=CC=C(N)C=C3)C=C2)(C(F)(F)F)C(F)(F)F)C=C1
• IUPAC Name: 4,4'-{(1,1,1,3,3,3-Hexafluoropropane-2,2-diyl)bis[(4,1-phenylene)oxy]}dianiline
• InChIKey: HHLMWQDRYZAENA-UHFFFAOYSA-N
• INCHI: InChI=1S/C27H20F6N2O2/c28-26(29,30)25(27(31,32)33,17-1-9-21(10-2-17)36-23-13-5-19(34)6-14-23)18-3-11-22(12-4-18)37-24-15-7-20(35)8-16-24/h1-16H,34-35H2
• Isómeros SMILES: C1=CC(=CC=C1C(C2=CC=C(C=C2)OC3=CC=C(C=C3)N)(C(F)(F)F)C(F)(F)F)OC4=CC=C(C=C4)N
• WGK Alemania: 3
• RTECS: CY1213000
• Peso molecular: 518.45
• Reaxy-Rn: 8879443
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8879443&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Diphenylmethanes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Diphenylmethanes
• Intermediate Tree Nodes: Not available
• Direct Parent: Diphenylmethanes
• Alternative Parents: Diphenylethers Diarylethers Phenoxy compounds Phenol ethers Aniline and substituted anilines Primary amines Organopnictogen compounds Organofluorides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Diphenylmethane - Diphenylether - Diaryl ether - Phenoxy compound - Phenol ether - Aniline or substituted anilines - Ether - Amine - Primary amine - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Alkyl fluoride - Organic oxygen compound - Hydrocarbon derivative - Alkyl halide - Organopnictogen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as diphenylmethanes. These are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Solubilidad: Insoluble in water, soluble in methanol
• Punto de fusión (°C): 159-163°C

Referencias

1. Lidong Cao, Yaqing Wen, Xingzhong Fang, Guofei Chen.  (2023)  Synthesis of highly thermoplastic polyamide-imides with high transparency and low coefficient of thermal expansion.  POLYMER,      [PMID:] [10.1016/j.polymer.2023.126093]

2. Chaoying Liao, Zhaozhu Zhang, Yaohui He, Junya Yuan, Mingming Yang, Peilong Li, Wei Jiang, Yongmin Liang, Weimin Liu.  (2025)  Bioinspired Antiwear Poly(urea-imide) Composites: Influence of Tribology on Polymer Crystal Structure.  Small,      [PMID:39780741] [10.1002/smll.202408249]

3. Chaoying Liao, Zhaozhu Zhang, Yaohui He, Mingming Yang, Junya Yuan, Peilong Li, Yongmin Liang.  (2025)  Liquid metal microcapsules induced formation of dual-layer tribofilm for enhanced wear resistance in fabric composites.  TRIBOLOGY INTERNATIONAL,      [PMID:] [10.1016/j.triboint.2025.110598]