17788-47-5

Basic information

• Product Name: 1,4-Naphthalenedione, 5-nitro-
• CAS NO: 17788-47-5
• Molecular Formula: C10H5NO4
• Molecular Weight: 203.154
• Mol File: 17788-47-5.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 1,4-Naphthalenedione, 5-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Naphthalenedione, 5-nitro-(17788-47-5)
• EPA Substance Registry System: 1,4-Naphthalenedione, 5-nitro-(17788-47-5)

Safety Data

• Hazardous Substances Data: 17788-47-5(Hazardous Substances Data)

Usage

Appearance

Bright yellow crystalline powder

Solubility

Insoluble in water and most organic solvents

Primary use

Intermediate in the production of dyes and pigments

Specific application

Precursor to yellow pigment Pigment Yellow 10

Additional uses

Manufacture of pharmaceuticals, chemical reagent in organic synthesis

Antimicrobial properties

Exhibited in the compound

Antiviral properties

Shown to have potential in medical applications

Antioxidant effects

Demonstrated in the compound

Anti-inflammatory effects

Displayed by the compound

Potential therapeutic uses

Interest in the compound for its antioxidant and anti-inflammatory properties

Upstream product

• 54176-33-9 8-nitro-1,4-naphthoquinone-1-oxime 
• 7440-44-0 pyrographite 
• 67-56-1 methanol 
• 130-15-4 [1,4]naphthoquinone 
• 57478-35-0 5-nitro-1,4-naphthoquinone-1-oxime 
• 776-11-4 8-Nitro-1-hydroxy-naphthalin 
• 86-57-7 1-Nitronaphthalene 
• 6304-46-7 5-nitro-1-naphthol 

Downstream Products

• 68450-00-0 1,4,4a,9a-Tetrahydro-1-methyl-8-nitroanthrachinon 
• 1989-42-0 1,3-dimethoxy-9,10-anthraquinone 
• 82-45-1 1-amino-9,10-anthracenedione 
• 1417453-56-5 8-acetylamino-2-(cyclohex-1-enyl)benz[f]indole-4,9-dione 
• 1417453-54-3 3,5-bis(acetylamino)-2-(1-hydroxycyclohexylethynyl)-1,4-naphthoquinone 
• 1254329-60-6 6-nitro-3,4-bis(phenylamino)-1-pyridin-2-yl-benzo[g]isoquinoline-5,10-dione 
• 1254329-59-3 9-nitro-3,4-bis(phenylamino)-1-pyridin-2-yl-benzo[g]isoquinoline-5,10-dione 
• 1254329-61-7 3,4-bis(4-bromophenylamino)-9-nitro-1-pyridin-2-yl-benzo[g]isoquinoline-5,10-dione 
• 1254329-62-8 3,4-bis(4-bromophenylamino)-6-nitro-1-pyridin-2-yl-benzo[g]isoquinoline-5,10-dione 
• 82-34-8 1-nitroanthraquinone 
• 68450-02-2 8-Amino-1-methyl-1,2,3,4,9,10-hexahydro-anthracene-9,10-diol 
• 68450-03-3 5-Amino-1-methyl-1,2,3,4,9,10-hexahydro-anthracene-9,10-diol 
• 63038-00-6 5-aminonaphthalene-1,4-dione 

Relevant articles and documents

5-ARYLETHYNYL-1,4-NAPHTHOQUINONES

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Ruthenium(II)-Catalyzed Double Annulation of Quinones: Step-Economical Access to Valuable Bioactive Compounds

Double ruthenium(II)-catalyzed alkyne annulations of quinones were accomplished. Thus, a strategy is reported that provides step-economical access to valuable quinones with a wide range of applications. C?H/N?H activations for alkyne annulations of naphthoquinones provided challenging polycyclic quinoidal compounds by forming four new bonds in one step. The singular power of the thus-obtained compounds was reflected by their antileukemic activity.

1,2-Naphthoquinone-based Derivatives and and Methods for Preparing them

The present invention relates to a compound represented by chemical formula (1), a pharmaceutically acceptable salt, a hydrate, a solvate, a prodrug, a tautomer, an enantiomer, or a pharmaceutically acceptable diastereomer thereof, a preparing method thereof, and a medical composition having a treating or preventing effect of metabolic diseases containing the same. Here, R_1 to R_3, and X_1 to X_6 are the same as defined in a first claim.COPYRIGHT KIPO 2015