A89405
9-Anthracenecarboxylic acid
99%
Synonym(s):
9-Anthroic acid
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C15H10O2
CAS Number:
Molecular Weight:
222.24
Beilstein:
1875336
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
99%
form
powder
mp
213-217 °C (lit.)
λmax
254 nm at 0.1% in ethanol
SMILES string
OC(=O)c1c2ccccc2cc3ccccc13
InChI
1S/C15H10O2/c16-15(17)14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-9H,(H,16,17)
InChI key
XGWFJBFNAQHLEF-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
9-Anthracenecarboxylic acid can be used as a starting material to synthesize:
It can also be used as a cross-linking agent to functionalize organic second-order nonlinear optical materials to enhance poling efficiency and temporal stability.
- 9-Cyanoanthracene by reacting with cyanohydrins in the presence of a palladium catalyst.
- 6-Chloro-8-(9-anthracenyl)-9H-purine by Ag/SiO2 catalyzed reaction one-pot reaction with 6-chloro-4,5-pyrimidinediamine.
It can also be used as a cross-linking agent to functionalize organic second-order nonlinear optical materials to enhance poling efficiency and temporal stability.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Krisztina Váczi et al.
Naunyn-Schmiedeberg's archives of pharmacology, 388(1), 87-100 (2014-10-26)
Understanding the role of ionic currents in shaping the cardiac action potential (AP) has great importance as channel malfunctions can lead to sudden cardiac death by inducing arrhythmias. Therefore, researchers frequently use inhibitors to selectively block a certain ion channel
Bence Hegyi et al.
Journal of molecular and cellular cardiology, 109, 27-37 (2017-07-03)
The role of Ca2+-activated Cl- current (ICl(Ca)) in cardiac arrhythmias is still controversial. It can generate delayed afterdepolarizations in Ca2+-overloaded cells while in other studies incidence of early afterdepolarization (EAD) was reduced by ICl(Ca). Therefore our goal was to examine
Ag Loaded on SiO2 as an Efficient and Recyclable Heterogeneous Catalyst for the Synthesis of Chloro-8-substituted-9H-purines
Maddila S, et al.
Journal of Heterocyclic Chemistry, 53(1), 319-324 (2016)
Straightforward conversion of arene carboxylic acids into aryl nitriles by palladium-catalyzed decarboxylative cyanation reaction
Ouchaou K, et al.
Synlett, 2010(14), 2083-2086 (2010)
Mild and in situ photo-crosslinking of anthracene-functionalized poly (aryl ether ketone) for enhancing temporal stability of organic NLO materials
Tian Yanxin, et al.
J. Mater. Sci., 56(9), 5910-5923 (2021)
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