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2,3-bis(naphthalen-2-ylsulfanyl)naphthalene-1,4-dione is a naphthoquinone derivative featuring a unique molecular structure with two naphthalene rings connected by a sulfur atom. This chemical compound is of interest for its potential applications in various fields, including organic synthesis, material science, and pharmaceutical chemistry. Its distinctive structure and properties make it a valuable building block for the development of specialized organic molecules and materials.

18093-43-1

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18093-43-1 Usage

Uses

Used in Organic Synthesis:
2,3-bis(naphthalen-2-ylsulfanyl)naphthalene-1,4-dione is used as a key intermediate in the synthesis of complex organic molecules. Its unique structure allows for the formation of various functional groups and the creation of novel organic compounds with potential applications in different industries.
Used in Material Science:
In the field of material science, 2,3-bis(naphthalen-2-ylsulfanyl)naphthalene-1,4-dione is used as a building block for the development of new materials with specific properties. Its incorporation into polymers, for example, can lead to materials with improved thermal stability, electrical conductivity, or other desirable characteristics.
Used in Pharmaceutical Chemistry:
2,3-bis(naphthalen-2-ylsulfanyl)naphthalene-1,4-dione is used as a starting material or a structural component in the design and synthesis of new pharmaceutical compounds. Its unique structure and properties may contribute to the development of innovative drugs with improved efficacy, selectivity, or reduced side effects.
Used in Research and Development:
2,3-bis(naphthalen-2-ylsulfanyl)naphthalene-1,4-dione is utilized in research and development efforts to explore its potential applications in various scientific and technological fields. Further studies on 2,3-bis(naphthalen-2-ylsulfanyl)naphthalene-1,4-dione may lead to the discovery of new and innovative uses, expanding its relevance and impact in the scientific community.

Check Digit Verification of cas no

The CAS Registry Mumber 18093-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,9 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18093-43:
(7*1)+(6*8)+(5*0)+(4*9)+(3*3)+(2*4)+(1*3)=111
111 % 10 = 1
So 18093-43-1 is a valid CAS Registry Number.

18093-43-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-bis(naphthalen-2-ylsulfanyl)naphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names -

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

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More Details:18093-43-1 SDS

18093-43-1Downstream Products

18093-43-1Relevant academic research and scientific papers

A one-pot synthesis of 1,4-naphthoquinone-2,3-bis-sulfides catalysed by a commercial laccase

Wellington, Kevin W.,Bokako, Refiloe,Raseroka, Nelly,Steenkamp, Paul

, p. 2567 - 2576 (2013/02/23)

Oxidative C-S bond formation with aryl and alkyl thiols was catalysed under mild conditions in a reaction vessel open to air at pH 4.5 and 7.15 in the presence of a commercial laccase (Novozym 51003) and a co-solvent (DMF) to afford 1,4-naphthoquinone-2,3

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