A89405
9-Anthracenecarboxylic acid
99%
Synonym(s):
9-Anthroic acid
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About This Item
Empirical Formula (Hill Notation):
C15H10O2
CAS Number:
Molecular Weight:
222.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-964-9
Beilstein/REAXYS Number:
1875336
MDL number:
Assay:
99%
Form:
powder
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
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.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A89405-25G | 04061833400968 |
| A89405-5G | 04061831832501 |