CAS 66310-10-9

Pyridinium, 2,4,6-triphenyl-1-(phenylmethyl)-, tetrafluoroborate(1-)

Description:

Pyridinium, 2,4,6-triphenyl-1-(phenylmethyl)-, tetrafluoroborate(1-) is an organic compound characterized by its complex structure, which includes a pyridinium cation and a tetrafluoroborate anion. The pyridinium moiety is a positively charged nitrogen-containing heterocycle, while the tetrafluoroborate anion is a stable, non-coordinating anion commonly used in ionic liquids and as a counterion in various chemical applications. This compound exhibits properties typical of ionic salts, such as high solubility in polar solvents and potential conductivity. The presence of multiple phenyl groups contributes to its stability and may influence its electronic properties, making it of interest in organic synthesis and materials science. Additionally, the compound's unique structure may impart specific reactivity patterns, making it useful in various chemical reactions, including those involving nucleophiles or electrophiles. Overall, this compound exemplifies the interplay between organic chemistry and ionic interactions, showcasing the versatility of pyridinium derivatives in synthetic applications.

Formula: C₃₀H₂₄N・BF₄

N-BENZYL-2,4,6-TRIPHENYL PYRIDINIUM TETRAFLUOROBORATE

CAS: 66310-10-9

Formula: C₃₀H₂₄BF₄N

Purity: 97%

Color and Shape: Solid

Molecular weight: 485.3229

Ref: IN-DA00FAPN

N-Benzyl-2,4,6-triphenylpyridinium tetrafluoroborate

CAS: 66310-10-9

N-Benzyl-2,4,6-triphenylpyridinium tetrafluoroborate

Purity: ≥95%

Color and Shape: White Powder

Molecular weight: 485.32g/mol

Ref: 54-PC31766

1-Benzyl-2,4,6-triphenylpyridin-1-ium tetrafluoroborate

CAS: 66310-10-9

Purity: 97%

Molecular weight: 485.3299865722656

Ref: 10-F750441

N-Benzyl-2,4,6-triphenyl pyridinium tetrafluoroborate

CAS: 66310-10-9

N-Benzyl-2,4,6-triphenyl pyridinium tetrafluoroborate is a molecule that regulates transcriptional activity. It can be used to isolate regulatory genes from different organisms and identify the specific genes that regulate the expression of other genes. The algorithm for this process is a stepwise, stereoselective, aerobic search. This process starts with an algorithm that identifies the best possible match between the gene sequence and the database sequences. The algorithm then transfers to another stepwise and stereoselective search of the database until it finds a match. The process ends when there are no more matches in the database or when all possible combinations have been searched. N-Benzyl-2,4,6-triphenyl pyridinium tetrafluoroborate has been shown to activate Staphylococcus aureus at very low concentrations but does not cause activation of mammalian cells at these concentrations.

Formula: C₃₀H₂₄N·BF₄

Purity: Min. 95%

Molecular weight: 485.32 g/mol

Ref: 3D-FB66085