Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

793221

Sigma-Aldrich

9-Mesityl-10-phenylacridinium tetrafluoroborate

Synonym(s):

9-Mesityl-10-phenylacridinium tetrafluoroborate, 10-Phenyl-9-(2,4,6-trimethylphenyl)acridinium tetrafluoroborate

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C28H24BF4N
CAS Number:
Molecular Weight:
461.30
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.22

form

solid

reaction suitability

core: acridinium
reagent type: catalyst
reaction type: Photocatalysis

mp

>200 °C

photocatalyst activation

450 nm

SMILES string

CC(C=C1C)=CC(C)=C1C2=C3C(C=CC=C3)=[N+](C4=CC=CC=C4)C5=CC=CC=C52.F[B-](F)(F)F

InChI

1S/C28H24N.BF4/c1-19-17-20(2)27(21(3)18-19)28-23-13-7-9-15-25(23)29(22-11-5-4-6-12-22)26-16-10-8-14-24(26)28;2-1(3,4)5/h4-18H,1-3H3;/q+1;-1

InChI key

LGNMSOXRNBFBGX-UHFFFAOYSA-N

Application

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Articles

While Markovnikov alkene reactivity is very well developed and utilized commonly in the synthesis of commodity and research chemicals, catalytic access to the anti-Markovnikov-selective adducts is a much less-developed endeavor.

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.

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