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1,2,3,4,5,6-Hexa-O-benzyl-myo-inositol is a complex organic compound derived from myo-inositol, a naturally occurring cyclohexane-based sugar alcohol. 1,2,3,4,5,6-hexa-O-benzyl-myo-inositol is characterized by the presence of six benzyl groups attached to each of the six hydroxyl groups of myo-inositol, resulting in a highly substituted and sterically hindered structure. The benzyl groups are phenylmethyl moieties, which contribute to the compound's increased lipophilicity and stability. This chemical modification is often employed in synthetic chemistry to protect the hydroxyl groups during complex organic synthesis, particularly in the preparation of pharmaceuticals and other bioactive compounds. The hexa-O-benzyl-myo-inositol serves as an intermediate in the synthesis of various inositol derivatives, which are important in cellular signal transduction and other biological processes.

6382-98-5

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6382-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6382-98-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,8 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6382-98:
(6*6)+(5*3)+(4*8)+(3*2)+(2*9)+(1*8)=115
115 % 10 = 5
So 6382-98-5 is a valid CAS Registry Number.

6382-98-5Relevant academic research and scientific papers

Syntheses of penta-O-benzyl-myo-inositols, O-β-L-arabinosyl-(1 → 2)sn-myo-inositol, O-α-D-galactosyl-(1 → 3)-sn-myo-inositol, and O-α-D-galactosyl-(1 → 6)-O-α-D-galactosyl-(1 → 3)-sn-myo-inositol

Koto,Hirooka,Yoshida,Takenaka,Nagamitsu,Sakurai,Zen,Yago,Tomonaga

, p. 2521 - 2529 (2007/10/03)

Two-step conversions of myo-inositol into (±)-2,3,4,5,6- and 1,3,4,5,6-penta-O-benzyl-myo-inositols are described. Starting from these monohydroxy derivatives of myo-inositol, O-β-L-arabinopyranosyl-(1→2)-sn-myo-inositol from Japanese green tea, Camellia sinensis, and O-α-D-galactopyranosyl-(1→3)-sn-myo-inositol (galactinol) as well as its homolog, O-α-D-galactopyranosyl-(1→6(II))-galactinol, were synthesized by way of the in situ activating glycosylation procedure.

Concerning the reactivities of the C-1, C-2 and C-6 hydroxy groups of myo-inositol

Anilkumar, Gopinadhan Nair,Jia, Zhaozhong J.,Kraehmer, Ralf,Fraser-Reid, Bert

, p. 3591 - 3596 (2007/10/03)

Regioselectivities in the reactions of the three contiguous free hydroxy groups at C-6, C-1, and C-2 of 3,4,5-tri-O-benzyl-D-myo-inositol have been examined. Stannylene activation permits selective alkylation and esterification at C-1; however, acyl migra

Practical synthesis of a differentially protected myo-inositol

Kornienko, Alexander,Turner, David I.,Jaworek, Christine H.,D'Alarcao, Marc

, p. 2783 - 2786 (2007/10/03)

An enantiospecific synthesis of 3,4,5-tri-O-benzyl-6-O- triisopropylsilyl-D-myo-inositol from D-xylose is reported. The synthesis features a diastereofacially selective SmI2-promoted pinacol cyclization.

Synthesis of novel vitamin C phosphodiesters: Stability and antioxidant activity

Morisaki, Kazuo,Ozaki, Shoichiro

, p. 123 - 138 (2007/10/03)

A novel series of hybrid L-ascorbic acid (vitamin C) phosphodiesters linked at the C-2 hydroxyl group with other biologically active substances, namely myo-inositol, arbutin, 4-hydroxy-L-proline, and glycolic acid were synthesized, and their thermal stability and reducing activity against free radicals were estimated in vitro. All of the phosphodiesters exhibited high thermal stabilities; however, their antioxidant activities in vitro were generally lower than that of vitamin C.

Synthesis of -Labelled and Unlabelled 2-Deoxy-2-fluoro-myo-inositol and 1-Deoxy-1-fluoro-scyllo-inositol for Use in Studies of the Phosphoinositide Cycle

Lowe, Gordon,McPhee, Fiona

, p. 1249 - 1253 (2007/10/02)

2-Deoxy-2-fluoro-myo-inositol and 1-deoxy-1-fluoro-scyllo-inositol have been synthesized in their unlabelled and tritiated forms in order to study their potential as inhibitors of the phosphoinositide cycle.

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