22255-29-4

Basic information

• Product Name: 1-Hydroxy-2-hydroxymethyl-3-((3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-anthraquinone
• CAS NO: 22255-29-4
• Molecular Weight: 432.384
• Mol File: 22255-29-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 778.9±60.0 °C(Predicted)
• Density: 1.673±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-Hydroxy-2-hydroxymethyl-3-((3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-anthraquinone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Hydroxy-2-hydroxymethyl-3-((3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-anthraquinone(22255-29-4)
• EPA Substance Registry System: 1-Hydroxy-2-hydroxymethyl-3-((3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-anthraquinone(22255-29-4)

Safety Data

• Hazardous Substances Data: 22255-29-4(Hazardous Substances Data)

Usage

General Description

1-Hydroxy-2-hydroxymethyl-3-((3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-anthraquinone is a chemical compound that contains a hydroxy group, a hydroxymethyl group, and an anthraquinone core. The compound also includes a tetrahydropyran ring with multiple hydroxy and hydroxymethyl groups attached. This complex structure gives the molecule potential for various biological activities, including antioxidant, anti-inflammatory, and anticancer properties. It has applications in the pharmaceutical and chemical industries due to its potential therapeutic effects. The compound's intricate structure and potential biological activities make it a subject of interest for further research and development.

Upstream product

• 29706-59-0 lucidin-3-primeveroside 

Downstream Products

• 478-08-0 1,3-dihydroxy-2-hydroxymethyl-9,10-anthraquinone 

Relevant articles and documents

Antifeedant activity of an anthraquinone aldehyde in Galium aparine L. against Spodoptera litura F.

The insect antifeedant anthraquinone aldehyde nordamnacanthal (1,3-dihydroxy-anthraquinone-2-al) was identified in Galium aparine L., and isolated from the root powder of akane (Rubia akane), a member of the Rubiaceae. Structure-activity relationship (SAR) studies using a series of anthraquinone analogues suggested that the aldehyde group on the anthraquinone was more important than the quinone moiety for antifeedant activity against the common cutworm (Spodoptera litura). High levels of nordamnacanthal were found in the seed leaf stage and in callus tissue induced from seedlings of G. aparine, but its concentration decreased with plant development. Since these compounds are natural pigments for dying textiles, we also evaluated the antifeedant activity against the carpet beetle (Attagenus japonicus), a textile pest was also evaluated. While nordamnacanthal had strong antifeedant activity against the common cutworm, it did not show any antifeedant activity against the carpet beetle. The most effective antifeedant against the carpet beetle was the major constituent in the extract of R. trictorum, lucidin- 3 - O-primeveroside, a food pigment. 2002 Elsevier Science Ltd. All rights reserved.