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Sieber Linker

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CAS:3722-51-8
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CAS:3722-51-8
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Sieber Linker manufacturers

  • Sieber Linker
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  • 2024-04-15
  • CAS:3722-51-8
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  • Purity: 99%
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  • SieberLinker
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  • 2023-08-30
  • CAS:3722-51-8
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  • Sieber Linker
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  • $0.00 / 1KG
  • 2022-09-23
  • CAS:3722-51-8
  • Min. Order: 1KG
  • Purity: 98%
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Sieber Linker Basic information
Product Name:Sieber Linker
Synonyms:SIEBER LINKER;SALOR-INT L254835-1EA;6-HYDROXY-3-FLUORONE;3-HYDROXY-XANTHEN-9-ONE;3-HYDROXYXANTHONE;SIEBER LINKER,3-HYDROXY-XANTHEN-9-ONE;3-HYDROXY-XANTHEN-9-ONE SIEBER LINKER 99+%;SIEBER LINKER, 99% MIN.
CAS:3722-51-8
MF:C13H8O3
MW:212.2
EINECS:1312995-182-4
Product Categories:Linkers for Solid Phase Synthesis;Linkers for solid phase synthesis;linker
Mol File:3722-51-8.mol
Sieber Linker Structure
Sieber Linker Chemical Properties
Melting point 243 °C
Boiling point 403.9±24.0 °C(Predicted)
density 1.395±0.06 g/cm3(Predicted)
storage temp. Store at 0°C
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
pka7.52±0.20(Predicted)
form Solid
color White to Orange to Green
InChIInChI=1S/C13H8O3/c14-8-5-6-10-12(7-8)16-11-4-2-1-3-9(11)13(10)15/h1-7,14H
InChIKeyXCJHDJAODLKGLG-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C=CC=C2)OC2=C1C=CC(O)=C2
CAS DataBase Reference3722-51-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
HS Code 29329900
MSDS Information
Sieber Linker Usage And Synthesis
Chemical PropertiesWhite to off-white or grey powder
UsesSieber linker (3-Hydroxyxanthen-9-one) is a natural product of the trifluoroacetic acid group found in Hypericum sampsonii and Rhachidosorus mesosorus. It has antiplatelet and anti-inflammatory properties. It also inhibits the expression of tumour necrosis factor-α (TNF-α) in mice. The synthesis of TNF-α is inhibited by Sieber linker, which may be due to its ability to inhibit the enzyme phosphodiesterase 4 (PDE4). Sieber linker also inhibits the binding of PDL1 to dinucleotide phosphate (DNP) and has an inhibitory effect on cancer cells. This molecule can be used for the treatment of infectious diseases, such as malaria and tuberculosis, since it inhibits protein synthesis in bacteria.
Synthesis Reference(s)Tetrahedron, 43, p. 3075, 1987 DOI: 10.1016/S0040-4020(01)86849-6
Purification MethodsPurify the xanthone by chromatography on SiO2 gel with pet ether/*benzene as eluent. Recrystallise it from *benzene or EtOH. The acetate has m 157-158o. [Itoh et al. J Am Chem Soc 107 4819 1985, Davies et al. J Org Chem 23 307 1958]. [Beilstein 18 H 46, 18 I 315, 18 II 29, 21 III/IV 601.]
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