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(3aR,4R,5R,6R,7R,7aS)-4,7-Bis-allyloxy-5,6-bis-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxole is a complex organic compound with a molecular formula of C27H32O6. It features a hexahydro-benzo[1,3]dioxole core, which is a type of benzene derivative with two oxygen atoms in a six-membered ring. The compound has two allyl groups attached to the 4 and 7 positions, providing it with a double bond and a reactive site for further chemical reactions. Additionally, it has two benzyloxy groups at the 5 and 6 positions, which are benzyl ether groups that can protect hydroxyl groups in organic synthesis. The 2,2-dimethyl groups at the hexahydro-benzo[1,3]dioxole core contribute to the compound's stability and lipophilicity. This chemical is primarily used in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals, due to its unique structure and reactivity.

98906-38-8

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98906-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98906-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,9,0 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 98906-38:
(7*9)+(6*8)+(5*9)+(4*0)+(3*6)+(2*3)+(1*8)=188
188 % 10 = 8
So 98906-38-8 is a valid CAS Registry Number.

98906-38-8Relevant academic research and scientific papers

The Allyl Group for Protection in Carbohydrate Chemistry. Part 18. Allyl and Benzyl Ethers of myo-Inositol. Intermediates for the Synthesis of myo-Inositol Triphosphates

Gigg, Jill,Gigg, Roy,Payne, Sheila,Conant, Robert

, p. 423 - 430 (2007/10/02)

Racemic 1,2:4,5-di-O-isopropylidene-myo-inositol was converted into racemic 1,2,4-tri-O-benzyl-myo-inositol, 1,2,4-tri-O-p-methoxybenzyl-myo-inositol and 2,4,5-tri-O-benzyl-myo-inositol using allyl groups for 'temporary' protection.The benzyl ethers are required as intermediates for the synthesis of the 'second messenger', inositol 1,4,5-triphosphate and its metabolite, inositol 1,3,4-triphosphate. 1,2,3,4-Tetra-O-benzyl-myo-inositol, and its two monoallyl and monoprop-1-enyl ethers, were also prepared as model compounds for phosphorylation studies of the vicinal 5,6-diol system which occurs in 1,2,4-tri-O-benzyl-myo-inositol.

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