126330-71-0

Basic information

• Product Name: 6-O-(2,3,4-tri-O-benzyl-L-rhamnopyranosyl)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose
• Synonyms: 6-O-(2,3,4-tri-O-benzyl-L-rhamnopyranosyl)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose
• CAS NO: 126330-71-0
• Molecular Weight: 676.804
• Mol File: 126330-71-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 6-O-(2,3,4-tri-O-benzyl-L-rhamnopyranosyl)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 6-O-(2,3,4-tri-O-benzyl-L-rhamnopyranosyl)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose(126330-71-0)
• EPA Substance Registry System: 6-O-(2,3,4-tri-O-benzyl-L-rhamnopyranosyl)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose(126330-71-0)

Safety Data

• Hazardous Substances Data: 126330-71-0(Hazardous Substances Data)

Upstream product

• 126330-69-6 2-pyridyl 2,3,4-tri-O-benzyl-1-thio-α,β-L-rhamnopyranoside 
• 4064-06-6 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 103368-09-8 2,3,4-tri-O-benzyl-β-L-rhamnopyranose 1-O-trichloroacetimidate 
• 5158-64-5 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide 
• 136984-94-6 2-pyridyl 2,3,4-tri-O-acetyl-1-thio-α/β-L-rhamnoyranoside 
• 100-39-0 benzyl bromide 
• 210426-02-1 2,3,4-tri-O-benzyl-L-rhamnopyranose 
• 215794-84-6 pyrimidin-2-yl 2,3,4,-tri-O-acetyl-1-thio-α-L-rhamnopyranoside 
• 63753-91-3 3,4-di-O-acetyl-1,2-O-methoxyethylidene-β-L-rhamnopyranose 
• 215794-89-1 pyrimidin-2-yl 2,3,4,-tri-O-benzyl-1-thio-α-L-rhamnopyranoside 

Relevant articles and documents

1,2-cis-β-Mannopyranoside Formation by the Dimethylphosphinothioate Method

1,2-cis-β-Mannopyranosides were obtained predominantly by reactions of mannopyranosyl dimethylphosphinothioate derivatives with several alcohols in the presence of iodine and a catalytic amount of triphenylmethyl perchlorate as the activator in benzene.

Stereoselective synthesis of β-rhamnopyranosides via gold(i)-catalyzed glycosylation with 2-alkynyl-4-nitro-benzoate donors

Stereoselective β-rhamnopyranosylation remains a challenge, due to the unfavorable anomeric effect and steric hindrance of the C2-substituent; herein, this challenge is addressed with a gold(I)-catalyzed SN2-like glycosylation protocol employin

New Synthetic Methods and Reagents for Complex Carbohydrates. VIII. Steroselective α- and β-Mannopyranoside Formation from Glycosyl Dimethylphosphinothioates with the C-2 Axial Benzyloxyl Group

The reactions of mannopyranosyl dimethylphosphinothioates and alcohols using silver perchlorate as an activator in the presence of molecular sieves 4A in benzene at room temperature gave the 1,2-trans-α-mynnopyranosides in good yields.On the other hand, 1