Skip to Content
Merck
All Photos(2)

Key Documents

909327

Sigma-Aldrich

2,7-Dimethoxy-9-mesityl-10-methylacridinium tetrafluoroborate

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C25H26BF4NO2
Molecular Weight:
459.28
UNSPSC Code:
12352101
NACRES:
NA.22

form

powder

reaction suitability

reaction type: Photocatalysis
reagent type: catalyst

SMILES string

[F-][B+3]([F-])([F-])[F-].O(C=1C=CC2=C(C1)C(=C3C=C(OC)C=CC3=[N+]2C)C4=C(C=C(C=C4C)C)C)C

InChI

InChI=1S/C25H26NO2.BF4/c1-15-11-16(2)24(17(3)12-15)25-20-13-18(27-5)7-9-22(20)26(4)23-10-8-19(28-6)14-21(23)25;2-1(3,4)5/h7-14H,1-6H3;/q+1;-1

InChI key

NEMWBWBWRDTDNA-UHFFFAOYSA-N

Application

Robust acridinium-based photocatalyst for use as an alternative to transition-metal-based photocatalysts with higher chemical stability and attenuated redox potential.

Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Related Content

The Nicewicz lab is focused on the discovery of new and powerful reaction methodologies that proceed via the intermediacy of highly reactive cation radical species. Included in these transformations are anti-Markovnikov selective additions of amines, alcohols, carboxylic acids, amides and mineral acids to alkenes.

Photoredox catalysis utilizes photocatalysts in the presence of visible light to form an array of synthetic transformations including, but not limited to, cross-coupling, C-H functionalization, alkene and arene functionalization, and trifluoromethylation.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service