Phosphine,tris[3,5-bis(trifluoromethyl)phenyl]-

Product Information

Molecular Formula:
C24H9 F18 P
Molecular Weight:
670.27
Description
Phosphine,tris[3,5-bis(trifluoromethyl)phenyl]- is a vital compound in the biomedical industry used for various purposes. It acts as a catalyst in organic synthesis reactions and is employed in the development of pharmaceutical drugs targeting specific diseases. This compound exhibits exceptional stability and reactivity, making it an essential tool in drug discovery and synthesis processes. Its unique properties make it suitable for treating various diseases and developing novel therapeutic interventions.
Synonyms
TRI[3,5-DI(TRIFLUOROMETHYL)PHENYL]PHOSPHINE; TRIS[3,5-BIS(TRIFLUOROMETHYL)PHENYL]PHOSPHINE; TRIS[3,5-DI(TRIFLUOROMETHYL)PHENYL]PHOSPHINE; TRIS[BIS(3,5-TRIFLUOROMETHYL)PHENYL]PHOSPHINE; TRIS[3,5-BIS(TRIFLUOROMETHYL)PHENYL]PHOSPHINE 97%; Tris[3,5-bis(trifluorom
IUPAC Name
tris[3,5-bis(trifluoromethyl)phenyl]phosphane
Canonical SMILES
C1=C(C=C(C=C1C(F)(F)F)P(C2=CC(=CC(=C2)C(F)(F)F)C(F)(F)F)C3=CC(=CC(=C3)C(F)(F)F)C(F)(F)F)C(F)(F)F
InChI
InChI=1S/C24H9F18P/c25-19(26,27)10-1-11(20(28,29)30)5-16(4-10)43(17-6-12(21(31,32)33)2-13(7-17)22(34,35)36)18-8-14(23(37,38)39)3-15(9-18)24(40,41)42/h1-9H
InChI Key
ITJHLZVYLDBFOJ-UHFFFAOYSA-N
Boiling Point
128-130°C 0,5mm
Melting Point
95°C
Flash Point
Not applicable
Purity
95%
Appearance
yellow-brown
Storage
Keep under Nitrogen

Safety Information

Hazards
H315 - H319 - H335
Precautionary Statement
P302 + P352 - P305 + P351 + P338

Computed Properties

XLogP3
9.9
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
18
Rotatable Bond Count
3
Exact Mass
670.0154442 g/mol
Monoisotopic Mass
670.0154442 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
43
Formal Charge
0
Complexity
741
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-112062772-A Organic compound, organic photoelectric element using same and application 2020-09-10
CN-112142752-A Organic compound, organic photoelectric element using same and application 2020-09-10
CN-112062774-A Organic compound and organic electroluminescent device using same 2020-09-09
CN-112062753-A Organic compound, organic photoelectric element using same and application 2020-09-09
CN-112079844-A Organic compound, organic photoelectric element using same and application 2020-09-09
CN-114149422-A Condensed ring compound and organic electronic device 2020-09-08
WO-2022003040-A1 Process for treating keratin fibers using particular amino acids in high concentration 2020-06-30
JP-2021126617-A Carbon dioxide reduction catalyst 2020-02-13
JP-2021109157-A Carbon compound reduction catalyst 2020-01-14
JP-2021053622-A Carbon compound reduction catalyst 2019-09-24

Literatures

PMID Publication Date Title Journal
21557356 2011-06-14 Synthesis, characterisation and application of iridium(III) photosensitisers for catalytic water reduction Chemistry (Weinheim an der Bergstrasse, Germany)
20024326 2010-01-07 Ortho-C-H borylation of benzoate esters with bis(pinacolato)diboron catalyzed by iridium-phosphine complexes Chemical communications (Cambridge, England)
16129706 2005-09-05 Type I interferons act directly on CD8 T cells to allow clonal expansion and memory formation in response to viral infection The Journal of experimental medicine
16161315 2005-01-01 [Regulation of glycemia, just where and when in the aged?] Journees annuelles de diabetologie de l'Hotel-Dieu
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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