1307876-21-6

Basic information

• Product Name: 3-O-[2-O-benzyl-3,4-di-O-acetyl-β-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-α-L-rhamnopyranoside]-4'-O-benzylkaempferol
• Synonyms: 3-O-[2-O-benzyl-3,4-di-O-acetyl-β-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-α-L-rhamnopyranoside]-4'-O-benzylkaempferol
• CAS NO: 1307876-21-6
• Molecular Weight: 912.898
• Mol File: 1307876-21-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-O-[2-O-benzyl-3,4-di-O-acetyl-β-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-α-L-rhamnopyranoside]-4'-O-benzylkaempferol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-O-[2-O-benzyl-3,4-di-O-acetyl-β-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-α-L-rhamnopyranoside]-4'-O-benzylkaempferol(1307876-21-6)
• EPA Substance Registry System: 3-O-[2-O-benzyl-3,4-di-O-acetyl-β-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-α-L-rhamnopyranoside]-4'-O-benzylkaempferol(1307876-21-6)

Safety Data

• Hazardous Substances Data: 1307876-21-6(Hazardous Substances Data)

Upstream product

• 1307876-13-6 3,5-di-O-acetyl-7-O-allylkaempferol 
• 1307876-14-7 3,5-di-O-acetyl-4'-O-benzyl-7-O-allylkaempferol 
• 1307876-15-8 4'-O-benzyl-7-O-allylkaempferol 
• 1307876-19-2 3-O-[2-O-benzyl-3,4-di-O-acetyl-β-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-α-L-rhamnopyranoside]-4'-O-benzyl-7-O-allylkaempferol 
• 1307876-11-4 7-O-allylkaempherol 
• 1307876-12-5 3,4',5-tri-O-acetyl-7-O-allylkaempferol 
• 520-18-3 kaempferol 
• 100-39-0 benzyl bromide 

Downstream Products

• 1307876-22-7 3-O-[2-O-benzyl-3,4-di-O-acetyl-β-L-arabinopyranosyl-(1->4)-2,3-di-O-acetyl-α-L-rhamnopyranoside]-4'-O-benzyl-7-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranoside)kaempferol 

Relevant articles and documents

Efficient synthesis of a bisglycosyl kaempferol from fagonia taeckholmiana

The first total synthesis of kaempferol-3-O-β-L-arabinopyranosyl-( 1→4)-α-L-rhamnopyranoside-7-O-α-L-rhamnopyranoside (1), a 3, 7-triglycosylflavone, which was isolated from the aerial parts of Fagonia taeckholmiana, was accomplished in 13 steps and 9.2% overall yield from commercially available kaempferol. We efficiently employed phase-transfer- catalyzed (PTC) glycosylation for the construction of phenol glycosides. Applying this approach will allow the preparation of derivatives for further study of structureactivity relationships (SAR).