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About This Item
Empirical Formula (Hill Notation):
C11H12O2
CAS Number:
Molecular Weight:
176.21
Beilstein:
2208389
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
99%
form
solid
mp
59-63 °C (lit.)
functional group
ketone
SMILES string
COc1ccc2CCCC(=O)c2c1
InChI
1S/C11H12O2/c1-13-9-6-5-8-3-2-4-11(12)10(8)7-9/h5-7H,2-4H2,1H3
InChI key
GABLTKRIYDNDIN-UHFFFAOYSA-N
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Application
7-methoxy-1-tetralone was used in the synthesis of 2,7-dimethoxy-1-tetralone, substituted derivatives of 3a,4,5,6-tetrahydrosuccinimido[3,4-b]acenaphthen-10-one and 13H-benzo[6-7]indolo[3,2-c]quinolines.
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
Regulatory Information
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13H-benzo [6-7] indolo [3, 2-c] quinolines (B [6, 7] IQ): optimization of their DNA triplex-specific stabilization properties.
Schmitt P, et al.
Chemical Communications (Cambridge, England), 9, 763-764 (2000)
Substituted Derivatives of 3a, 4, 5, 6-Tetrahydrosuccinimido [3, 4-b] Acenaphthen-10-one.
Campaigne E and Weddleton RF.
Proceedings of the Indian Academy of Sciences - Section A, 95 (2013)
The reaction of 1-tetralones with thallium trinitrate supported on clay: ring contraction vs alpha-oxidation.
Ferraz H, et al.
Journal of the Brazilian Chemical Society, 12(5), 680-684 (2001)
Tian-Min Wang et al.
Journal of separation science, 40(17), 3440-3452 (2017-07-07)
As a traditional medicinal plant, Juglans mandshurica has been used for the treatment of cancer. Different organs of this plant showed anti-tumor activity in clinic and laboratory. Comparative identification of constituents in different plant organs is essential for investigation of
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