Name: Name:2,4,6-Triphenylpyrylium tetrafluoroborate
Brand: AABLOCKS
SKU: AA00374O
Rating: 90 (10 reviews)

2,4,6-Triphenylpyrylium tetrafluoroborate demonstrates its utility as a sensitizer in various photochemical reactions. In one application, it acts as a sensitizer to facilitate the photooxidation of catechol, showcasing its role in promoting light-induced chemical transformations. Moreover, it serves as a key component in the synthesis of N-alkylpyridinium photosensitizers by reacting with different chiral amines. This highlights its versatility in the preparation of specialized photosensitive compounds for diverse applications. For researchers utilizing photoreactors, 2,4,6-Triphenylpyrylium tetrafluoroborate proves compatible with a range of photoreactor models, including Penn PhD and SynLED 2.0, providing a convenient solution for carrying out photochemical reactions efficiently.

Catalog No.: AA00374O

448-61-3 | 2,4,6-Triphenylpyrylium tetrafluoroborate

Pack Size： 1g

Purity： ≥97%

in stock

$10.00 $7.00

Pack Size： 5g

Purity： ≥97%

in stock

$23.00 $16.00

Pack Size： 10g

Purity： 95%

in stock

$32.00 $23.00

Pack Size： 25g

Purity： 95%

in stock

$78.00 $55.00

Pack Size： 100g

Purity： 95%

in stock

$311.00 $218.00

Quantity

- +

Add to Card

Order Now

bulk Quotation Request

Technical Information

Catalog Number: AA00374O

Chemical Name: 2,4,6-Triphenylpyrylium tetrafluoroborate

CAS Number: 448-61-3

Molecular Formula: C23H17BF4O

Molecular Weight: 396.1851

MDL Number: MFCD11617925

SMILES: c1ccc(cc1)c1cc([o+]c(c1)c1ccccc1)c1ccccc1.F[B-](F)(F)F

Properties

Form: Solid

MP: 250-251 °C(lit.)

Stability: Moisture Sensitive

Storage: Inert atmosphere;2-8℃;

Complexity: 353

Covalently-Bonded Unit Count: 2

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 29

Hydrogen Bond Acceptor Count: 5

Hydrogen Bond Donor Count: 0

Isotope Atom Count: 0

Rotatable Bond Count: 3

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

Literature fold

Title: The role of aromatic radical cations and benzylic cations in the 2,4,6-triphenylpyrylium tetrafluoroborate photosensitized oxidation of ring-methoxylated benzyl alcohols in CH2Cl2 solution.

Journal: The Journal of organic chemistry20041210

Application fold

2,4,6-Triphenylpyrylium tetrafluoroborate demonstrates its utility as a sensitizer in various photochemical reactions. In one application, it acts as a sensitizer to facilitate the photooxidation of catechol, showcasing its role in promoting light-induced chemical transformations.

Moreover, it serves as a key component in the synthesis of N-alkylpyridinium photosensitizers by reacting with different chiral amines. This highlights its versatility in the preparation of specialized photosensitive compounds for diverse applications.

For researchers utilizing photoreactors, 2,4,6-Triphenylpyrylium tetrafluoroborate proves compatible with a range of photoreactor models, including Penn PhD and SynLED 2.0, providing a convenient solution for carrying out photochemical reactions efficiently.