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5-methoxy-8-methyl-3,4-dihydronaphthalen-1(2H)-one is a complex chemical compound that features a naphthalene ring with a 3,4-dihydronaphthalen core. It is a ketone derivative characterized by the presence of a methoxy group at the 5th position and a methyl group at the 8th position. 5-methoxy-8-methyl-3,4-dihydronaphthalen-1(2H)-one, existing in the 1(2H)-one form, is of interest in the fields of organic synthesis and pharmaceutical research due to its unique structural features.

53863-68-6

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53863-68-6 Usage

Uses

Used in Organic Synthesis:
5-methoxy-8-methyl-3,4-dihydronaphthalen-1(2H)-one is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of derivatives, making it a valuable building block in the development of new chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-methoxy-8-methyl-3,4-dihydronaphthalen-1(2H)-one is used as a starting material for the development of potential drug candidates. Its complex structure and functional groups offer opportunities for the design of novel therapeutic agents with specific biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 53863-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,6 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53863-68:
(7*5)+(6*3)+(5*8)+(4*6)+(3*3)+(2*6)+(1*8)=146
146 % 10 = 6
So 53863-68-6 is a valid CAS Registry Number.

53863-68-6Relevant academic research and scientific papers

Synthesis of 8-methyl-1-tetralone, a potential intermediate for (±)-platyphyllide

Poon, Po S.,Bedoya, Liadis,Churio, Gabriel J.,Banerjee, Ajoy K.

, p. 1747 - 1753 (2015/02/19)

An alternative method for the synthesis of the 8-methyl-1-tetralone from the commercially available 5-methoxy-1-tetralone has been developed. The transformation involves eight steps and affords an overall yield 25%.

2-Aminomethyl-3,4-dihydronaphthalenes

-

, (2008/06/13)

Compounds of the formula STR1 and pharmaceutically acceptable salts thereof, wherein X and Y are independently H, F, Cl, Br, alkyl having up to four carbons, or alkoxy having up to four carbons, but X and Y are not both H, and Z is a secondary or tertiary amino group, are useful as analgesics and tranquillizing agents for mammals.

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