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1-Propenyl 2,4,6-tri-O-benzyl-3-O-(1-propenyl)-α-D-glucopyranose is a complex organic compound that belongs to the class of glycosides. It is a derivative of α-D-glucopyranose, a monosaccharide, with three benzyl groups attached to the 2, 4, and 6 positions of the sugar ring, and two propenyl groups attached to the 1 and 3 positions. 1-propenyl 2,4,6-tri-O-benzyl-3-O-(1-propenyl)-α-D-glucopyranose is significant in the field of organic chemistry and carbohydrate chemistry, as it serves as a building block for the synthesis of more complex oligosaccharides and glycoconjugates. The presence of the propenyl groups allows for further functionalization and modification, making it a versatile intermediate in the preparation of bioactive compounds and pharmaceuticals. The benzyl protecting groups are commonly used in organic synthesis to prevent unwanted side reactions and can be removed under specific conditions when the desired product is achieved.

77388-93-3

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77388-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77388-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,8 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77388-93:
(7*7)+(6*7)+(5*3)+(4*8)+(3*8)+(2*9)+(1*3)=183
183 % 10 = 3
So 77388-93-3 is a valid CAS Registry Number.

77388-93-3Relevant 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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