590368-07-3

Basic information

• Product Name: toralactone 9-O-yl 6-O-acetyl-2,3,4-tri-O-benzoyl-β-D-glucopyranoside
• Synonyms: toralactone 9-O-yl 6-O-acetyl-2,3,4-tri-O-benzoyl-β-D-glucopyranoside
• CAS NO: 590368-07-3
• Molecular Weight: 788.761
• Mol File: 590368-07-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: toralactone 9-O-yl 6-O-acetyl-2,3,4-tri-O-benzoyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: toralactone 9-O-yl 6-O-acetyl-2,3,4-tri-O-benzoyl-β-D-glucopyranoside(590368-07-3)
• EPA Substance Registry System: toralactone 9-O-yl 6-O-acetyl-2,3,4-tri-O-benzoyl-β-D-glucopyranoside(590368-07-3)

Safety Data

• Hazardous Substances Data: 590368-07-3(Hazardous Substances Data)

Upstream product

• 137334-39-5 6-O-acetyl-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl bromide 
• 3686-57-5 2,4-dimethoxy-6-methylbenzoic acid 
• 71602-63-6 10-hydroxy-7,9-dimethoxy-3-methyl-1H-benzo[g]isochromen-1-on-9-O-methyllactone 
• 41743-74-2 Toralactone 
• 590368-14-2 6-O-acetyl-2,3,4-tri-O-benzoyl-D-glucopyranosyl (N-phenyl)trifluoroacetimidate 
• 485807-57-6 6-O-acetyl-2,3,4-tri-O-benzoyl-D-glucopyranosyl trichloroacetimidate 

Downstream Products

• 590368-09-5 toralactone 9-O-yl 6-O-acetyl-2,3,4-tri-O-benzoyl-β-D-glucopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-β-D-glucopyranoside 
• 119170-52-4 cassiaside C 
• 590367-94-5 toralactone 9-O-yl 2,3,4-tri-O-benzoyl-β-D-glucopyranoside 

Relevant articles and documents

Total synthesis of the antiallergic naphtho-α-pyrone tetraglucoside, cassiaside C2, isolated from Cassia seeds

Toralactone 9-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl-(1→3)- P-D-glucopyranosyl-(1-6)-β-D-glucopyranoside (1, cassiaside C2), isolated from Cassia obtusifolia L. and showing strong antiallergic activity, was concisely synthesized employing glycosyl trifluoroacetimidates as glycosylation agents. The unique naphtho-α-pyrone structure of toralactone (5) was constructed by condensation of orsellinate 8 with pyrone 9 in the presence of LDA as developed by Staunton and co-workers. The naphthol of toralactone showed minimal reactivity as an acceptor and was screened with various glycosyl donors. It is finally concluded that sacrifice of an excess amount of the trifluoroacetimidate or trichloroacetimidate donors (6f/6g, 6.0 equiv) in the presence of a catalytic amount of TMSOTf (0.05 and 0.3 equiv, respectively) afforded excellent yields of the coupling product, which was otherwise only a minor product under a variety of conditions examined.