164186
7-Methoxy-2-tetralone
97%
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About This Item
Empirical Formula (Hill Notation):
C11H12O2
CAS Number:
Molecular Weight:
176.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-954-1
Beilstein/REAXYS Number:
1953198
MDL number:
Assay:
97%
Form:
solid
InChI key
XEAPZXNZOJGVCZ-UHFFFAOYSA-N
InChI
1S/C11H12O2/c1-13-11-5-3-8-2-4-10(12)6-9(8)7-11/h3,5,7H,2,4,6H2,1H3
SMILES string
COc1ccc2CCC(=O)Cc2c1
assay
97%
form
solid
bp
124-126 °C/1.5 mmHg (lit.)
density
1.13 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Application
7-Methoxy-2-tetralone was used in the synthesis of 2-bromo-3,4-dihydro-7-methoxy-1-naphthaldehyde and 2-substituted octahydrobenzo[f]quinolines.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
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Dajie Li et al.
Bioorganic & medicinal chemistry, 11(17), 3795-3805 (2003-08-07)
Substituted benzo[i]phenanthridines that have incorporated within their structure an 8,9-methylenedioxy group can exhibit topoisomerase I-targeting activity. Structure-activity studies were performed to examine the influence of saturation at the 11,12-positions of several substituted 8,9-methylenedioxybenzo[i]phenanthridines. The activities of these dihydro analogues were
J C Craig et al.
Journal of medicinal chemistry, 32(5), 961-968 (1989-05-01)
A series of 2-substituted octahydrobenzo[f]quinolines has been synthesized and assayed for dopamine agonist activity. Only the compounds corresponding to the beta-rotameric conformation of dopamine showed biphasic activity in competition binding studies with the radioligand [3H]spiroperidol. These findings suggest that the
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