A89405
9-蒽甲酸
99%
别名:
9-蒽羧酸
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关于此项目
经验公式（希尔记法）:
C15H10O2
化学文摘社编号:
分子量:
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-蒽甲酸可用作合成以下物质的原料：
它还可用作交联剂，用于有机二阶非线性光学材料的功能化修饰，以提高极化效率和时间稳定性。
- 在钯催化剂存在的情况下与氰醇反应合成的9-氰基蒽。
- 通过与 6-氯-4,5-嘧啶二胺进行的Ag/SiO2 催化一锅法反应合成的6-氯-8-(9-蒽基)-9H-嘌呤。
它还可用作交联剂，用于有机二阶非线性光学材料的功能化修饰，以提高极化效率和时间稳定性。
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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
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)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| A89405-25G | 04061833400968 |
| A89405-5G | 04061831832501 |