6130-58-1

Basic information

• Product Name: kaempferol 3-O-α-L-rhamnopyranosyl-(1→6)-β-D-galactopyranoside
• CAS NO: 6130-58-1
• Molecular Weight: 594.526
• Mol File: 6130-58-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: kaempferol 3-O-α-L-rhamnopyranosyl-(1→6)-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: kaempferol 3-O-α-L-rhamnopyranosyl-(1→6)-β-D-galactopyranoside(6130-58-1)
• EPA Substance Registry System: kaempferol 3-O-α-L-rhamnopyranosyl-(1→6)-β-D-galactopyranoside(6130-58-1)

Safety Data

• Hazardous Substances Data: 6130-58-1(Hazardous Substances Data)

Upstream product

• 57526-56-4 kaempherol 3-O-[α-L-rhamnopyranosyl-(1->6)]-β-D-glucopyranosyl-7-O-α-L-rhamnopyranoside 
• 131559-51-8 kaempferol 3-O-(2^G-xylosylrutinoside)-7-O-glucoside 
• 135095-52-2 3-O-[(2-O-β-D-galactopyranosyl-6-O-α-L-rhamnopyranosyl)-β-D-glucopyranosyl]-kaempferol 
• 131573-90-5 kaempferol 3-O-β-D-<2^G-O-β-D-xylopyranosyl-6^G-O-α-L-rhamnopyranosyl>glucopyranoside 
• 131559-50-7 kaempferol 3-O-(2^G-glucosylrutinoside)-7-O-glucoside 
• 34336-18-0 7-O-β-D-glucopyranosyloxy-4',5-dihydroxy-3-[O-α-L-rhamnopyranosyl-(1->6)-3-O-β-D-glucopyranosyloxy]flavone 
• 131573-90-5 kaempferol 3-O-(2^G-xylosylrutinoside) 

Downstream Products

• 26184-96-3 rutinose 
• 520-18-3 kaempferol 
• 634-74-2 D-rhamnose 
• 50-99-7 D-glucose 
• 3615-41-6 L-Rhamnose 
• 4205-23-6 D-gulose 
• 1318780-82-3 C₃₀H₁₈O₁₃ 
• 61198-83-2 1,2,3,4-tetra-O-benzoyl-6-desoxy-α-L-mannopyranose 
• 552-74-9 6-O-α-L-rhamnopyranosyl-β-D-glucopyranose 
• 58947-55-0 biorobin nonaacetate 
• 2280-44-6 D-Glucose 
• 73-34-7 D-rhamnose 
• 33978-17-5 pelargonidin 3-O-β-rutinoside 

Relevant articles and documents

Kaempferol and its glycosides from Equisetum silvaticum L. from the khanty-mansi autonomous area

Three flavonoids were isolated from the aerial part of the wood horsetail (Equisetum silvaticum L.); two of them were found for the first time. The compounds were identified as kaempferol, kaempferol 3-O-β-D-galactopyranosyl-7-O-α-L-rhamnopyranoside and kaempferol 3-O-rutinosyl-7-O-L-rhamnopyranoside on the basis of the chemical transformations and IR, UV, 1H-NMR and mass spectra.

Two flavonol glycosides from seeds of Camellia sinensis.

Two novel flavonol triglycosides, camelliaside A and B, have been isolated from seeds of Camellia sinensis. The structures were determined to be kaempferol 3-O-[2-O-beta-D- galactopyranosyl-6-O-alpha-L-rhamnopyranosyl]-beta-D-glucopyranoside and kaempferol 3-O-[2-O-beta- D-xylopyranosyl-6-O-alpha-L-rhamnopyranosyl]-beta-D-glucopyranoside on the basis of spectroscopic, chemical and enzymatic studies. These types of interglycosidic linkages, Gal(1----2)[Rha(1----6)]Glc and Xyl(1----2)[Rha(1----6)]Glc, have not been reported previously in flavone and flavonol glycosides.

Constituents of Cupuliferae, II. - A New Acylated Flavonoid Glycoside from Castanea sativa Mill.

From leaves of Castanea sativa Mill. in addition to tiliroside , 3>, a new acylated flavonoid glycoside has been isolated and identified as kaempferol 3-O-Glc-(p-coumaroyl)-α-L-rhamnopyranosyl-(1->6)-β-D-glucopyranoside> (1).