15075-11-3

Basic information

• Product Name: 3-O-methyl-D-xylose
• Synonyms: 3-O-methyl-D-xylose
• CAS NO: 15075-11-3
• Molecular Weight: 164.158
• Mol File: 15075-11-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-O-methyl-D-xylose(CAS DataBase Reference)
• NIST Chemistry Reference: 3-O-methyl-D-xylose(15075-11-3)
• EPA Substance Registry System: 3-O-methyl-D-xylose(15075-11-3)

Safety Data

• Hazardous Substances Data: 15075-11-3(Hazardous Substances Data)

Upstream product

• 915213-96-6 fuscocineroside B 
• 1082071-34-8 3-O-[3-O-methyl-β-D-glucopyranosyl-(1->3)-β-D-glucopyranosyl-(1->4)-β-D-quinovopyranosyl-(1->2)-4-O-sodiumsulfato-β-D-xylopyranosyl]-22-oxo-9(11)-holostene-3β,12α,25-triol 
• 1033617-26-3 3-O-[3-O-methyl-β-D-glucopyranosyl-(1->3)-β-D-glucopyranosyl-(1->4)-β-D-quinovopyranosyl-(1->2)-4-O-sodiumsulfato-β-D-xylopyranosyl]-22-oxo-9(11)-holostene-3β,12α,17α-triol 

Downstream Products

• 35522-76-0 O³-methyl-D-threo-[2]pentosulose-bis-phenylhydrazone 
• 35506-61-7 ((3aR,5R,6S,6aR)-6-Methoxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-methanol 
• 107280-94-4 O³-methyl-D-threo-[2]pentosulose-bis-(4-bromo-phenylhydrazone) 
• 21569-62-0 D-erythro-3-deoxy-pentonic acid 
• 21569-63-1 3-Desoxy-D-threo-pentonsaeure 

Relevant articles and documents

Two new holostan-type triterpene glycosides from the sea cucumber Bohadschia marmorata Jaeger

Two new holostan-type triterpene glycosides, 17-hydroxy fuscocineroside B (1) and 25-hydroxy fuscocineroside B (2), together with a known triterpene glycoside, fuscocineroside B (3) were isolated from the sea cucumber Bohadschia marmorata JAEGER. The structures of the new triterpene glycosides were elucidated on the basis of spectroscopic analyses and chemical reactions. Compounds 1 and 3 showed considerable antifungal activities against six strains.

Two antifungal active triterpenoid saponins from the seeds of Lathyrus plants

Two novel triterpenoid glycosides have been isolated from butanolic seeds extract of two varieties of Lathyrus plants, i.e. Lathyrus ratan and Lathyrus aphaca. Their structures were elucidated as 3-O-[β-D-glucuronopyranosyl- (1→4)-α-L-arabinopyranosyl-(1→2)-α-L-arabinopyranosyl] -olean-11,13 (18)-dien-28-oic acid (1) and 3-O-{β-D-xylopyranosyl-(1 → 2)-β-D-glcopyranosyl-(1→4)-[β-D-glucopyranosyl-(1→2)]- α-D-xylopyranosyl}-2, 16-dihydroxy-4-hydroxymethyl urs-12-en-28-oic acid (2) on the basis of spectral evidences, i.e. FTIR, 1H-NMR, 13C-NMR, ESI-MS and FAB-MS data. The isolated saponins were tested for their antifungal activity. Compound 1 showed maximum inhibition against Colletotrichum dematium (77.8%), whereas compound 2 showed maximum inhibition against Alternaria alternata (53.9%).