126179
9,10-Dihydroanthracene
97%
Synonym(s):
Dihydroanthracene
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About This Item
Empirical Formula (Hill Notation):
C14H12
CAS Number:
Molecular Weight:
180.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-336-1
Beilstein/REAXYS Number:
1364575
MDL number:
Assay:
97%
Form:
solid
Quality Level
assay
97%
form
solid
bp
312 °C (lit.)
mp
103-107 °C (lit.)
density
0.88 g/mL at 25 °C (lit.)
SMILES string
C1c2ccccc2Cc3ccccc13
InChI
1S/C14H12/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-8H,9-10H2
InChI key
WPDAVTSOEQEGMS-UHFFFAOYSA-N
General description
9,10-Dihydroanthracene causes the transfer hydrogenation of C60 and C70 in the presence of [7H]benzanthrene catalyst. It was oxidatively aromatized to the corresponding anthracene in the presence of molecular oxygen as an oxidant and activated carbon as a promoter in xylene.
Application
9,10-Dihydroanthracene(DHA) has been used in a study to assess the hydrogen abstraction capability of valence-delocalized iron complex with DHA in MeCN.
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Natsuki Nakamichi et al.
The Journal of organic chemistry, 68(21), 8272-8273 (2003-10-11)
Substituted 9,10-dihydroanthracenes were oxidatively aromatized to the corresponding anthracenes effectively by using molecular oxygen as an oxidant and activated carbon (Darco KB, Aldrich, Inc.) as a promoter in xylene.
[7H] Benzanthrone, a catalyst for the transfer hydrogenation of C60 and C70 by 9, 10-dihydroanthracene.
Gerst M, et al.
Tetrahedron Letters, 34(48), 7729-7732 (1993)
Pengfei Sun et al.
Small (Weinheim an der Bergstrasse, Germany), 16(3), e1906462-e1906462 (2019-12-24)
Lithium primary batteries are still widely used in military, aerospace, medical, and civilian applications despite the omnipresence of rechargeable Li-ion batteries. However, these current primary chemistries are exclusively based on inorganic materials with high cost, low energy density or severe
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 126179-100G | 04061833063422 |
| 126179-5G | 04061838723895 |