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1,3-Anhydro-2,4,6-tri-O-benzyl-β-D-glucopyranose is a complex organic compound that belongs to the class of carbohydrates, specifically a glycoside. It is derived from β-D-glucopyranose, a monosaccharide, by protecting three of its hydroxyl groups with benzyl groups. The 1,3-anhydro part of the name indicates that the compound has an anhydro ring structure formed between the first and third carbon atoms, which results in the removal of a water molecule. 1,3-anhydro-2,4,6-tri-O-benzyl-β-D-glucopyranose is often used in organic synthesis, particularly in the preparation of more complex oligosaccharides and glycoconjugates, due to its stability and the ease with which the benzyl protecting groups can be removed under specific conditions to reveal the underlying hydroxyl groups for further reactions.

76543-11-8

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76543-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76543-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,4 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76543-11:
(7*7)+(6*6)+(5*5)+(4*4)+(3*3)+(2*1)+(1*1)=138
138 % 10 = 8
So 76543-11-8 is a valid CAS Registry Number.

76543-11-8Downstream Products

76543-11-8Relevant academic research and scientific papers

SYNTHESIS OF A SUBSTITUTED 2,6-DIOXABICYCLOHEPTANE, 1,3-ANHYDRO-2,4,6-TRI-O-BENZYL-β-D-GLUCOPYRANOSE

Ito, Hiroshi,Eby, Ronald,Kramer, Steven,Schuerch, Conrad

, p. 193 - 202 (2007/10/02)

1,3-Anhydro-2,4,6-tri-O-benzyl-β-D-glucopyranose has been synthesized by ring closure of 2,4,6-tri-O-benzyl-α-D-glucopyranosyl chloride via two reaction sequences.The preferable method has allyl 3-O-allyl D-glucopyranoside as key intermediate.This appears to be the first example of an anhydro sugar derivative with the 2,6-dioxabicycloheptane skeleton.

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