2,3,4,6-Tetra-O-benzyl-alpha-D-glucopyranosyl trichloroacetimidate

• CAT Number: L036852
• CAS Number: 74808-09-6
• Molecular Formula: C36H36Cl3NO6
• Molecular Weight: 685.00
• Purity: ≥95%
• IUPAC Name: [(2R,3R,4S,5R,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl] 2,2,2-trichloroethanimidate
• InChI: InChI=1S/C36H36Cl3NO6/c37-36(38,39)35(40)46-34-33(44-24-29-19-11-4-12-20-29)32(43-23-28-17-9-3-10-18-28)31(42-22-27-15-7-2-8-16-27)30(45-34)25-41-21-26-13-5-1-6-14-26/h1-20,30-34,40H,21-25H2/t30-,31-,32+,33-,34-/m1/s1
• InChIKey: LMICALCPRSCSMO-BGSSSCFASA-N
• SMILES: C1=CC=C(C=C1)COC[C@@H]2[C@H]([C@@H]([C@H]([C@H](O2)OC(=N)C(Cl)(Cl)Cl)OCC3=CC=CC=C3)OCC4=CC=CC=C4)OCC5=CC=CC=C5

2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate（Cat No.:L036852）is a protected sugar derivative widely used as a glycosyl donor in carbohydrate synthesis. It features a D-glucopyranose ring with benzyl protecting groups at the 2, 3, 4, and 6 positions, and a trichloroacetimidate group at the anomeric center, enabling selective glycosidic bond formation under mild acidic conditions. This compound appears as a white to off-white solid and is commonly employed in the synthesis of oligosaccharides and glycoconjugates. Its stability and reactivity make it a valuable intermediate in medicinal chemistry and glycoscience research.