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(3aR,4S,5S,6R,7S,7aR)-4,5,7-Tris-benzyloxy-6-methoxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxole is a complex organic compound characterized by its unique molecular structure. It features a hexahydro-benzo[1,3]dioxole core, which is a type of benzene derivative with two oxygen atoms in a ring, forming a dioxole. The compound is adorned with three benzyloxy groups at the 4, 5, and 7 positions, which are benzyl ether functional groups derived from benzyl alcohol. Additionally, it has a methoxy group at the 6 position, contributing to its methoxy functionality. The 2,2-dimethyl groups at the hexahydro-benzo[1,3]dioxole core enhance the molecule's steric hindrance. The stereochemistry of the compound is defined by the 'R' and 'S' configurations at various carbon centers, indicating the three-dimensional arrangement of the molecule's atoms. This specific arrangement is crucial for its chemical properties and potential applications in fields such as pharmaceuticals or materials science.

80971-00-2

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80971-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80971-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,7 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80971-00:
(7*8)+(6*0)+(5*9)+(4*7)+(3*1)+(2*0)+(1*0)=132
132 % 10 = 2
So 80971-00-2 is a valid CAS Registry Number.

80971-00-2Relevant articles and documents

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.

The Allyl Group for Protection in Carbohydrate Chemistry. Part 20. Synthesis of 1L-1-O-Methyl-myo-inositol by Resolution of (+/-)-1,2,4-Tri-O-benzyl-myo-inositol

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

, p. 1757 - 1762 (2007/10/02)

Racemic 1,2,4-tri-O-benzyl-myo-inositol was prepared by two new routes from (+/-)-1,4-di-O-benzyl-5,6-O-isopropylidine-myo-inositol, one route involving the crystalline intermediate (+/-)-1-O-allyl-3,6-di-O-benzyl-4,5-O-isopropylidine-myo-inositol.Oxidati

Cyclitol Reactions, V. - Synthesis of Enantiomerically Pure Valienamine from Quebrachitol

Paulsen, Hans,Heiker, Fred R.

, p. 2180 - 2203 (2007/10/02)

An enantioselective synthesis of Valienamine (86) from quebrachitol (L-2O-methyl-chiro-inositol) (1) is described.Valienamine (86) is an unsaturated branched-chain aminocyclitol found in the central structural unit of the antidiabetic drug acarbose.Techniques for the introduction of side chains, azido groups, and double bonds into inositol systems are investigated.The methods developed in this connection are applied in the synthesis of valienamine.

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