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Benzyl 3,4,6-Tri-O-acetyl-2-benzamido-2-deoxy-β-D-glucopyranoside is a complex organic compound with the molecular formula C27H29NO8. It is a derivative of β-D-glucopyranoside, a monosaccharide, where the hydroxyl group at the 2-position is replaced by a benzamido group, and the hydroxyl groups at the 3, 4, and 6 positions are acetylated. Benzyl 3,4,6-Tri-O-acetyl-2-benzamido-2-deoxy-β-D-glucopyranoside is often used in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. Its structure features a benzyl group attached to the anomeric carbon, which can protect the reducing end of the sugar during chemical reactions, and the acetyl groups serve to protect the hydroxyl groups from unwanted side reactions. Benzyl 3,4,6-Tri-O-acetyl-2-benzamido-2-deoxy-β-D-glucopyranoside is significant in the field of carbohydrate chemistry due to its potential applications in the synthesis of biologically active molecules and the study of carbohydrate-mediated interactions.

4710-89-8

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4710-89-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4710-89-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,1 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4710-89:
(6*4)+(5*7)+(4*1)+(3*0)+(2*8)+(1*9)=88
88 % 10 = 8
So 4710-89-8 is a valid CAS Registry Number.

4710-89-8Downstream Products

4710-89-8Relevant academic research and scientific papers

Anomeric O-Alkylation, 11. Anomeric O-Alkylation of O-Unprotected Hexoses and Pentoses - Convenient Synthesis of Decyl, Benzyl, and Allyl Glycosides

Klotz, Wolfgang,Schmidt, Richard R.

, p. 683 - 690 (2007/10/02)

The base-promoted reaction of O-unprotected aldoses 1-6 with didecyl sulfate in DMPU affords decyl glycosides 1aα-6aα and 1aβ, 3aβ-6aβ in good overal yields.Similarly, the treatment of O-unprotected hexoses 1-4 and pentoses 5 and 6 with benzyl bromide and allyl bromide yields after subsequent O-acetylation monosaccharides 1cα-6cα, 1cβ, 3cβ-6cβ and 1dα-6dα, 1dβ, 3dβ-6dβ, respectively.The regio- and stereoselectivity in these reactions was determined by 1H-NMR spectroscopic data of the O-acetylated derivatives.Key Words: Aldoses, O-unprotected, glycoside formation / Anomeric oxides, alkylation / Alkylating agents, didecyl sulfate, benzyl bromide, allyl bromide / α-D-galacto-furanosides

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