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273937

6,7-Dimethoxy-1-tetralon

Name: 6,7-Dimethoxy-1-tetralon
Brand: ALDRICH

97%

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About This Item

Empirische Formel (Hill-System):

C₁₂H₁₄O₃

CAS-Nummer:

13575-75-2

Molekulargewicht:

206.24

MDL-Nummer:

MFCD00134100

UNSPSC-Code:

12352100

PubChem Substanz-ID:

24856554

NACRES:

NA.22

Assay

97%

Form

powder

mp (Schmelzpunkt)

98-100 °C (lit.)

Funktionelle Gruppe

ketone

SMILES String

COc1cc2CCCC(=O)c2cc1OC

InChI

1S/C12H14O3/c1-14-11-6-8-4-3-5-10(13)9(8)7-12(11)15-2/h6-7H,3-5H2,1-2H3

InChIKey

YNNJHKOXXBIJKK-UHFFFAOYSA-N

Allgemeine Beschreibung

6,7-Dimethoxy-1-tetralone reacts with 2-amino-4,5-dimethoxyacetophenone to form 5,6-dihydro-2,3,9,10-tetramethoxybenz[c]acridine.

Anwendung

Precursor to quinolines with dopaminergic activity, naphthols with anti-inflammatory activity, and benzophenanthridine alkaloids with antitumor activity.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

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Analysenzertifikate (COA)

Lot/Batch Number

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2-Aminotetralones: novel inhibitors of MurA and MurZ.

Colin J Dunsmore et al.

Bioorganic & medicinal chemistry letters, 18(5), 1730-1734 (2008-02-12)

Several 2-aminotetralones were identified as novel inhibitors of the bacterial enzymes MurA and MurZ. A number of these inhibitors demonstrated antibacterial activity against Staphylococcus aureus and Escherichia coli with MICs in the range 8-128 microg/ml. Based on structure-activity relationships we

The Journal of Organic Chemistry, 57, 5907-5907 (1992)

2-substituted-1-naphthols as potent 5-lipoxygenase inhibitors with topical antiinflammatory activity.

D G Batt et al.

Journal of medicinal chemistry, 33(1), 360-370 (1990-01-01)

The synthesis, biological evaluation, and structure-activity relationships of a series of 1-naphthols bearing carbon substituents at the 2-position are described. These compounds are potent inhibitors of the 5-lipoxygenase from RBL-1 cells and also inhibit bovine seminal vesicle cyclooxygenase. Structure-activity relationships

Synthesis and dopaminergic activity of 2-substituted octahydrobenzo[f]quinolines.

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

Substituted benz[a]acridines and benz[c]acridines as mammalian topoisomerase poisons.

D Makhey et al.

Bioorganic & medicinal chemistry, 8(5), 1171-1182 (2000-07-06)

Coralyne and several other synthetic benzo[a,g]quinolizium derivatives related to protoberberine alkaloids have exhibited activity as topoisomerase poisons. These compounds are characterized by the presence of a positively charged iminium group, which has been postulated to be associated with their pharmacological

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