Methyl galactofuranoside, TMS

• Formula: C₂₁H₅₂O₆Si₅
• Molecular weight: 541.0615
• IUPAC Standard InChI: InChI=1S/C21H52O6Si5/c1-28(2,3)22-16-17(24-29(4,5)6)18-19(25-30(7,8)9)20(26-31(10,11)12)21(23-18)27-32(13,14)15/h17-21H,16H2,1-15H3 Copy

  
• IUPAC Standard InChIKey: ZIWXPOHHTJQHTN-UHFFFAOYSA-N Copy
• Chemical structure:
  This structure is also available as a 2d Mol file
• Species with the same structure:
  • D-(+)-Talofuranose, pentakis(trimethylsilyl) ether (isomer 2)
  • D-(+)-Talofuranose, pentakis(trimethylsilyl) ether (isomer 1)
  • D-Allofuranose, pentakis(trimethylsilyl) ether
• Stereoisomers:
  • β-D-Galactofuranose, 1,2,3,5,6-pentakis-O-(trimethylsilyl)-
  • β-Gulofuranose, TMS
  • D(+)-Galactose, furanose, TMS
  • α-Galactofuranose, TMS
  • α-Altrofuranose, TMS
  • α-Gulofuranose, TMS
  • β-Allofuranose, TMS
  • β-Altrofuranose, TMS
• Information on this page:
  • Gas Chromatography
  • References
  • Notes
• Options:
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Gas Chromatography

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Normal alkane RI, non-polar column, temperature ramp

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References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Isidorov, Lech, et al., 2008
Isidorov, V.A.; Lech, P.; Zolciak, A.; Rusak, N.; Szczepaniak, L., Gas Chromatographic - nass spectrometric investigation of metabolites from the needles and roots of pine seedlings at early stages of pathogenic fungi Armillaria ostoyae attack, Trees, 2008, 22, 4, 531-542, https://doi.org/10.1007/s00468-008-0213-z . [all data]

Notes

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• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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