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The chemical compound "((2S,3aR,5R,6R,7S,7aR)-6,7-Bis-allyloxy-2-ethoxy-2-methyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-5-ylmethoxy)-tert-butyl-diphenyl-silane" is a complex, chiral molecule with a unique structure. It features a tetrahydro-[1,3]dioxolo[4,5-b]pyran core, which is a type of heterocyclic compound with oxygen atoms in a ring structure. The molecule is characterized by its stereochemistry, with the 'S' and 'R' designations indicating the specific three-dimensional arrangement of atoms around the chiral centers. It has two allyl ether groups attached to the 6 and 7 positions, an ethoxy group at the 2 position, and a methyl group, which contributes to its complexity. The molecule also includes a tert-butyl-diphenyl-silane moiety, which is a silane derivative with a tert-butyl group and two phenyl rings, providing additional structural diversity. ((2S,3aR,5R,6R,7S,7aR)-6,7-Bis-allyloxy-2-ethoxy-2-methyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-5-ylmethoxy)-tert-butyl-diphenyl-silane is likely to be used in advanced organic synthesis, potentially as a protecting group or in the formation of complex organic molecules due to its intricate structure and functional groups.

97576-41-5

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97576-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97576-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,7 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97576-41:
(7*9)+(6*7)+(5*5)+(4*7)+(3*6)+(2*4)+(1*1)=185
185 % 10 = 5
So 97576-41-5 is a valid CAS Registry Number.

97576-41-5Downstream Products

97576-41-5Relevant academic research and scientific papers

PREPARATION OF A GLYCOSYL DONOR SUITABLE FOR SYNTHESIS OF GLYCOPROTEIN "CORE" OLIGOSACCHARIDES

Liu, Charng-Ming,Warren, Christopher D.,Jeanloz, Roger W.

, p. 273 - 284 (2007/10/02)

2-O-Acetyl-3-O-allyl-4-O-benzyl-6-O-tert-butyldiphenylsilyl-D-glucopyranosyl chloride (14), a glycosyl donor suitable for synthesis of oligosaccharides corresponding to the N-glycoprotein saccharide "core", was synthesized by an efficient, six-stage route

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