129706-93-0

Basic information

• Product Name: methyl 3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside
• Synonyms: methyl 3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside
• CAS NO: 129706-93-0
• Molecular Weight: 372.418
• Mol File: 129706-93-0.mol
• Article Data: 60

Chemical Properties

• CAS DataBase Reference: methyl 3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside(129706-93-0)
• EPA Substance Registry System: methyl 3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside(129706-93-0)

Safety Data

• Hazardous Substances Data: 129706-93-0(Hazardous Substances Data)

Upstream product

• 14155-23-8 methyl 4,6-O-benzylidene-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 3162-96-7 methyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 2397-26-4 N,N-dimethyl(chlorophenylmethylene)ammonium chloride 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 3162-96-7 methyl 4,6-O-benzylidene-β-D-galactopyranoside 
• 76419-48-2 methyl 4,6-O-benzylidene-3-O-benzyl-α-D-glucopyranoside 
• 71117-37-8 (2R,4aR,6R,7R,8R,8aS)-6-Methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 86363-44-2 methyl 3-O-benzyl-4,6-O-benzylidene-β-D-mannopyranoside 
• 90593-22-9 Methyl 3-O-benzyl-4,6-O-benzylidene-2-O-<(trifluoromethyl)sulfonyl>-α-D-glucopyranoside 
• 65925-95-3 methyl 3-O-benzyl-4,6-O-benzylidene-β-D-arabino-hexopyranosid-2-ulose 
• 95587-91-0 methyl 3-O-benzyl-4,6-O-benzylidene-2-O-(trifluoromethanesulfonyl)-β-D-glucopyranoside 
• 100-44-7 benzyl chloride 

Downstream Products

• 129031-01-2 methyl 3-O-benzyl-4,6-O-benzylidene-2-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-β-D-galactopyranoside 
• 136632-92-3 methyl 4,6-O-benzylidene-3-O-benzyl-2-O-(methoxycarbonylmethyl)-α-D-mannopyranoside 
• 176915-90-5 methyl 3-O-benzyl-4,6-O-benzylidene-2-O-(6-O-acetyl-2-azido-13,4-di-O-benzyl-2-deoxy-α-mannopyranosyl)-α-D-glucopyranoside 
• 80680-58-6 methyl 3-O-benzyl-4,6-O-benzylidene-2-O-(N-imidazole-1-sulfonyl)-α-D-glucopyranoside 
• 107794-71-8 methyl 3-O-benzyl-4,6-O-benzylidene-2-O-(trifluoromethanefulfony)-β-D-glucopyranoside 
• 192936-02-0 methyl O-(2-O-acetyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1->2)-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 81348-19-8 methyl 2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranoside 

Relevant articles and documents

A Chiral Copper Catalyzed Site-Selective O-Alkylation of Carbohydrates

Highly regioselective alkylation of sugar hydroxyl groups has always been an important challenge in carbohydrate chemistry, especially for the selective alkylation of trans diols, there is no direct and efficient catalytic method so far. A chiral copper c

Regio/site-selective alkylation of substrates containing a: Cis -, 1,2- or 1,3-diol with ferric chloride and dipivaloylmethane as the catalytic system

In this study, we reported the regio/site-selective alkylation of substrates containing a cis-, 1,2- or 1,3-diol with FeCl3 as a key catalyst. A catalytic system consisting of FeCl3 (0.01-0.1 equiv.) and dipivaloylmethane (FeCl3/dipivaloylmethane = 1/2) was used to catalyze the alkylation in the presence of a base. The produced selectivities and isolated yields were similar to those obtained by methods using the same amount of FeL3 (L = acylacetone ligand) as the catalyst in most cases. The previously reported FeL3 catalysts for alkylation are not commercially available and have to be synthesized prior to use. In contrast, FeCl3 and dipivaloylmethane (Hdipm) are very common and inexpensive nontoxic reagents in the lab, thereby making the method much greener and easier to handle. Mechanism studies confirmed for the first time that FeCl3 initially reacts with two equivalents of Hdipm to form [Fe(dipm)3] in the presence of a base in acetonitrile, followed by the formation of a five or six-membered ring intermediate between [Fe(dipm)3] and two hydroxyl groups of the substrate. A subsequent reaction between the cyclic intermediate and the alkylating agent results in selective alkylation of the substrate.

One-pot synthesis of orthogonally protected sugars through sequential base-promoted/acid-catalyzed steps: A solvent-free approach with self-generation of a catalytic species

A varied set of solvent-free, one-pot synthetic sequences were developed to carry out the orthogonal protection of saccharide polyols. These sequences are composed of an initial regioselective benzylation, silylation or iodination (under mildly basic cond