Skip to Content
Merck
All Photos(1)

Documents

Safety Information

794260

Sigma-Aldrich

10-Phenyl-9(10H)-acridinone

95%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C19H13NO
CAS Number:
5472-23-1
Molecular Weight:
271.31
MDL number:
MFCD01463673
UNSPSC Code:
12352100
PubChem Substance ID:
329768435
NACRES:
NA.22

Quality Level

100

Assay

95%

form

solid

mp

274-279 °C

SMILES string

O=C1C2=C(C=CC=C2)N(C3=CC=CC=C3)C4=C1C=CC=C4

InChI

1S/C19H13NO/c21-19-15-10-4-6-12-17(15)20(14-8-2-1-3-9-14)18-13-7-5-11-16(18)19/h1-13H

InChI key

GOKIEMZASYETFM-UHFFFAOYSA-N

Application

Substrate was reported in the synthesis of oxirane derivatives through a two-step synthesis involving a McMurray reaction with 2-Adamantanone.

Other Notes

Oxiranes having an acridane structure as a novel chemiluminescent precursor: synthesis and chemiluminescent studies

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

794260-VAR:
794260-1G:
794260-BULK:

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

Related Content

Nicewicz Group – Professor Product Portal

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