585-91-1

Usage

Chemical Properties

White to off-white crystalline powder

InChI:InChI=1/C12H22O11/c13-1-3-5(15)7(17)9(19)11(21-3)23-12-10(20)8(18)6(16)4(2-14)22-12/h3-20H,1-2H2/t3-,4+,5-,6+,7+,8-,9-,10+,11-,12-/m1/s1

Upstream product

• 55676-46-5 2,3,4,6-tetra-O-acetyl-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-1-β-D-glucopyranoside 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 3947-62-4 2,3,4,6-tetra-O-acetyl-β-D-glucopyranose 
• 25320-59-6 tetra-O-benzyl glucopyranosyl chloride 
• 58781-27-4 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 

Downstream Products

• 18929-82-3 C₂₆H₃₀O₁₁ 
• 22554-66-1 α,β-Trehaloseoctaacetat 
• 38992-91-5 2,3,2',3'-tetra-O-benzyl-α,β-trehalose 
• 128242-05-7 C₅₄H₅₄O₁₁ 
• 39021-77-7 2,3,2',3'-tetra-O-benzyl-6,6'-di-O-p-tolylsulfonyl-α,β-trehalose 

Relevant academic research and scientific papers

Process for preparing compositions containing neotrehalose

Neotrehalose is prepared in a relatively high-yield by a process comprising allowing β-galactosidase to act on a solution containing lactoneotrehalose to form neotrehalose and recoverying the resultant neotrehalose. The neotrehalose is a non-reducing oligosaccharide having a satisfiable stability and a rich- and high-quality-sweetness and is assimilated and utilized as energy source in vivo when orally administered. Neotrehalose in the form of crystal has a satisfiable handleability because it is readily soluble in water and substantially free of hygroscopicity. These render neotrehalose very useful in the fields of food-, cosmetic- and pharmaceutical-industries.

SYNTHESIS OF UNSYMMETRICAL TREHALOSE ANALOGUES BY SILVER TRIFLUOROMETHANESULPHONATE PROMOTED GLYCOSYLATIONS

The coupling of benzoylated glucosyl bromides with 2,3,4,6-tetra-O-benzylated gluco, manno or galacto-pyranoses promoted by silver triflate is described, and the compositions of the crude reaction mixtures, determined by 13C NMR spectroscopy, are presente

Synthesis and glycosylation shift of 1,1'-disaccharides

Nineteen kinds of nonreducing 1,1'-disaccharides have synthesized by modified Koenigs-Knorr method, and characterized by NMR. The glycosylation shift of each anomeric carbon has been estimated.