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2-(benzylsulfanyl)-3-methylnaphthalene-1,4-dione is a chemical compound with a molecular formula C18H14O2S. It is a naphthalene derivative featuring a benzylsulfanyl group at the 2-position and a methyl group at the 3-position. 2-(benzylsulfanyl)-3-methylnaphthalene-1,4-dione also contains a 1,4-dione functional group, which suggests its potential reactivity in various organic reactions. Due to its diverse chemical reactivity and possible biological activity, it may have applications in organic synthesis, medicinal chemistry, and materials science.

2593-59-1

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2593-59-1 Usage

Uses

Used in Organic Synthesis:
2-(benzylsulfanyl)-3-methylnaphthalene-1,4-dione is used as a synthetic intermediate for the preparation of various complex organic molecules. Its 1,4-dione functional group allows for a range of reactions, making it a versatile building block in the synthesis of pharmaceuticals and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(benzylsulfanyl)-3-methylnaphthalene-1,4-dione is used as a potential lead compound for the development of new drugs. Its unique structure and reactivity may contribute to the discovery of novel therapeutic agents, particularly in the areas of cancer treatment and other diseases where its chemical properties could be exploited for targeted drug delivery or as a scaffold for new drug molecules.
Used in Materials Science:
2-(benzylsulfanyl)-3-methylnaphthalene-1,4-dione is used as a component in the development of new materials with specific properties. Its chemical structure may contribute to the creation of materials with tailored characteristics, such as improved conductivity, stability, or optical properties, which could be applied in various industries, including electronics, energy, and environmental protection.
Further research is needed to fully understand the properties and potential uses of 2-(benzylsulfanyl)-3-methylnaphthalene-1,4-dione, as its applications in these fields are currently speculative and based on its chemical structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 2593-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2593-59:
(6*2)+(5*5)+(4*9)+(3*3)+(2*5)+(1*9)=101
101 % 10 = 1
So 2593-59-1 is a valid CAS Registry Number.

2593-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzylsulfanyl-3-methylnaphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-(benzylsulfanyl)-3-methylnaphthalene-1,4-dione

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 -
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More Details:2593-59-1 SDS

2593-59-1Downstream Products

2593-59-1Relevant academic research and scientific papers

Silver-Catalyzed Direct Thiolation of Quinones by Activation of Aryl Disulfides to Synthesize Quinonyl Aryl Thioethers

Zhang, Cheng,McClure, Jesse,Chou, C. James

, p. 4919 - 4927 (2015/06/02)

A silver-catalyzed coupling reaction of quinones with aryl disulfides for the synthesis of quinonyl aryl thioethers is described. In the presence of AgOAc (0.2 equiv)/dppp (0.24 equiv) as the catalyst, (NH4)2S2O8/sub

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