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(1S,2R,3R,4S,5R,6S)-2,3,4,5-Tetrakis-benzyloxy-6-methoxy-cyclohexanol is a complex organic compound characterized by its unique stereochemistry and functional groups. It features a cyclohexane ring with four benzyloxy groups attached to the 2, 3, 4, and 5 positions, and a methoxy group at the 6 position. The compound's stereochemistry is defined by the R or S configuration at each chiral center, which influences its physical and chemical properties. This molecule is of interest in organic synthesis, particularly in the preparation of complex molecules and natural products, due to its ability to serve as a building block or intermediate. The benzyloxy groups protect the hydroxyl groups, allowing for further chemical manipulation, while the methoxy group at the 6 position provides additional functionality. (1S,2R,3R,4S,5R,6S)-2,3,4,5-Tetrakis-benzyloxy-6-methoxy-cyclohexanol is a testament to the precision required in organic chemistry, where the spatial arrangement of atoms significantly impacts the molecule's reactivity and potential applications.

6195-76-2

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6195-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6195-76-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6195-76:
(6*6)+(5*1)+(4*9)+(3*5)+(2*7)+(1*6)=112
112 % 10 = 2
So 6195-76-2 is a valid CAS Registry Number.

6195-76-2Relevant 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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