CAS 13406-29-6

tris(P-trifluoromethylphenyl)benzene

Description:

Tris(P-trifluoromethylphenyl)benzene, identified by its CAS number 13406-29-6, is an organic compound characterized by its unique molecular structure, which consists of a central benzene ring substituted with three P-trifluoromethylphenyl groups. This compound exhibits notable properties due to the presence of trifluoromethyl groups, which enhance its electron-withdrawing characteristics, thereby influencing its reactivity and stability. The trifluoromethyl groups also contribute to its hydrophobic nature, making it less soluble in polar solvents. Tris(P-trifluoromethylphenyl)benzene is often studied for its potential applications in materials science, particularly in the development of advanced polymers and liquid crystals, owing to its ability to modify thermal and optical properties. Additionally, its unique electronic properties may render it useful in electronic applications, such as organic semiconductors. Safety data indicates that, like many fluorinated compounds, it should be handled with care due to potential environmental and health impacts. Overall, this compound is of interest in both academic research and industrial applications.

Formula: C₂₁H₁₂F₉P

InChI: InChI=1/C21H12F9P/c22-19(23,24)13-1-7-16(8-2-13)31(17-9-3-14(4-10-17)20(25,26)27)18-11-5-15(6-12-18)21(28,29)30/h1-12H

InChI key: PXYCJKZSCDFXLR-UHFFFAOYSA-N

SMILES: c1cc(ccc1C(F)(F)F)P(c1ccc(cc1)C(F)(F)F)c1ccc(cc1)C(F)(F)F

Synonyms:

• Tris(4-trifluoromethylphenyl)phosphine
• Trisptrifluoromethylphenylphosphineminpaleyellowpowder
• Tris[4-(Trifluoromethyl)Phenyl]Phosphane

Tris[4-(trifluoromethyl)phenyl]phosphine

CAS: 13406-29-6

Formula: C₂₁H₁₂F₉P

Purity: >98.0%(GC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 466.29

Ref: 3B-T4115

Tris(p-trifluoromethylphenyl)phosphine, min. 97%

CAS: 13406-29-6

Tris(p-trifluoromethylphenyl)phosphine, min. 97%

Formula: (pCF₃C₆H₄)₃P

Purity: min. 97%

Color and Shape: pale yellow pwdr.

Molecular weight: 466.28

Ref: 08-15-8010

Tris[4-(trifluoromethyl)phenyl]phosphine

CAS: 13406-29-6

Tris[4-(trifluoromethyl)phenyl]phosphine

Formula: C₂₁H₁₂F₉P

Purity: 97%

Color and Shape: Solid

Molecular weight: 466.27936

Ref: 54-PC7919G

Tris(4-(trifluoromethyl)phenyl)phosphine

CAS: 13406-29-6

Formula: C₂₁H₁₂F₉P

Purity: 97%

Color and Shape: Solid

Molecular weight: 466.2794

Ref: IN-DA003V7P

Tris(4-(trifluoromethyl)phenyl)phosphine

CAS: 13406-29-6

Tris(4-(trifluoromethyl)phenyl)phosphine

Formula: C₂₁H₁₂F₉P

Purity: 97%

Molecular weight: 466.28

Ref: IN-DG155846

Tris(4-(trifluoromethyl)phenyl)phosphine

CAS: 13406-29-6

Purity: 97%

Color and Shape: Solid

Molecular weight: 466.29

Ref: 10-F791129

Tris(4-trifluoromethylphenyl)phosphine

Controlled Product

CAS: 13406-29-6

Formula: C₂₁H₁₂F₉P

Color and Shape: Neat

Molecular weight: 466.279

Ref: TR-T245170

Tris[4-(trifluoromethyl)phenyl]phosphine

CAS: 13406-29-6

Tris[4-(trifluoromethyl)phenyl]phosphine (TFPP) is a diphosphine ligand that binds to metal ions in the active site of enzymes. It has been shown to bind to methylenecyclopropanes, which are intermediates in the reaction of Grignard reagents with quinoline derivatives. TFPP is also able to form complexes with phosphines and other ligands, such as borane. The crystal structures of TFPP have been determined by x-ray diffraction studies. These structures show that TFPP is monosubstituted with four trifluoromethyl groups and one phosphorus atom.br>br> TFPP has also been shown to be an effective catalyst for reactions involving amides, such as hydroamination and acylation reactions. In addition, it was found that TFPP inhibits the growth of bacteria by inhibiting

Formula: C₂₁H₁₂F₉P

Purity: Min. 95%

Color and Shape: Solid

Molecular weight: 466.28 g/mol

Ref: 3D-FT100710