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6-hydroxy-7-methoxy-3,4-dihydronaphthalen-1(2H)-one is a complex organic compound with the molecular formula C11H12O3. It is a derivative of naphthalenone, characterized by the presence of a hydroxyl group (-OH) at the 6th position, a methoxy group (-OCH3) at the 7th position, and a dihydro (partially hydrogenated) structure in the 3,4 positions. 6-hydroxy-7-methoxy-3,4-dihydronaphthalen-1(2H)-one is known for its potential applications in the synthesis of various pharmaceuticals and natural products due to its unique structure and functional groups. It is typically synthesized through chemical reactions and can be found in research settings focused on organic chemistry and drug development.

15288-02-5

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15288-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15288-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,8 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15288-02:
(7*1)+(6*5)+(5*2)+(4*8)+(3*8)+(2*0)+(1*2)=105
105 % 10 = 5
So 15288-02-5 is a valid CAS Registry Number.

15288-02-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hydroxy-7-methoxy-3,4-dihydro-2H-naphthalen-1-one

1.2 Other means of identification

Product number -
Other names 2,3-Dihydro-6-hydroxy-7-methoxy-1(4H)-naphthalinon

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15288-02-5 SDS

15288-02-5Relevant academic research and scientific papers

Formation and composition of new optically active compounds

-

, (2008/06/13)

The present invention is directed to tetrahydronaphthalene derivatives of α-conindendrin, β-conindendrin, sikkimotoxin, and podophyllotoxin having at least one methyleneoxy bridge wherein the oxygen atom extends to the benzhydrylic carbon atom.

Directed, DDQ-Promoted Benzylic Oxygenations of Tetrahydronaphthalenes

Ramdayal, Frank D.,Kiemle, David J.,LaLonde, Robert T.

, p. 4607 - 4609 (2007/10/03)

Positional preferences for para benzylic oxygenation of tetrahydronaphthalenes by 2,3-dichloro5,6-dicyano-1,4-benzoquinone (DDQ)-aqueous dioxane were investigated by comparing the tetralone products from 6-hydroxy-7-methoxy- and 6-acetoxy-7-methoxy-1,2,3,

Direct Synthesis of Benzophenanthridines and Benzophenanthridones via SRN1 Reactions

Beugelmans, Rene,Chastanet, Jacqueline,Ginsburg, Helene,Quintero-Cortes, Leticia,Roussi, Georges

, p. 4933 - 4938 (2007/10/02)

A straightforward and high-yield route to the 11,12-dihydrobenzophenanthridine (3) and 11,12-dihydrobenzophenanthridone (14) ring systems is based upon an SRN1 reaction between 2-halobenzylamines 1 or 2-halobenzoic acids 11 and enolates derived from tetralones 2.The efficient dehydrogenation of 3 or 14 gives the benzophenthridines 4 or benzophenanthridones 15.Use of properly substituted reactants leads to nitidine, avicine, and fagaronine and to analogues of those natural products.

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