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1,3:4,6-di-O-benzylidene-D-threo-2,5-hexodiulose is a complex organic compound with the molecular formula C20H22O5. It is a derivative of D-threo-2,5-hexodiulose, a ketose sugar, where the hydroxyl groups at positions 1, 3, 4, and 6 are protected by benzylidene groups. 1,3:4,6-di-O-benzylidene-D-threo-2,5-hexodiulose is often used in organic synthesis and carbohydrate chemistry as a protecting group for the hydroxyl groups, which can be removed under certain conditions to regenerate the parent sugar. The benzylidene protection is crucial for preventing unwanted side reactions and ensuring the selective modification of specific functional groups in the molecule.

80018-66-2

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80018-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80018-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,1 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80018-66:
(7*8)+(6*0)+(5*0)+(4*1)+(3*8)+(2*6)+(1*6)=102
102 % 10 = 2
So 80018-66-2 is a valid CAS Registry Number.

80018-66-2Relevant academic research and scientific papers

Total synthesis of brevetoxin B. 2. Second generation strategies and construction of the dioxepane region [DEFG]

Nicolaou,Theodorakis,Rutjes,Sato,Tiebes,Xiao,Hwang,Duggan,Yang,Couladouros,Sato,Shin,He,Bleckman

, p. 10239 - 10251 (2007/10/03)

The second generation strategy for the total synthesis of brevetoxin B (1) is presented. According to this strategy, the heptacyclic [ABCDEFG] phosphonium iodide 4 and the tricyclic [IJK] aldehyde 3 were defined as the precursors for the brevetoxin B skel

SYNTHESIS AND SOME REACTIONS OF 1,3:4,6-DI-O-BENZYLIDENE-D-threo-2,5-HEXODIULOSE

Baggett, Neil,Stribblehill, Peter

, p. 41 - 58 (2007/10/02)

Oxidation of 1,3:4,6-di-O-benzylidene-D-mannitol in ethyl acetate with ruthenium tetroxide gave the corresponding diketone as its hydrate, which was dehydrated to the free diketone.These compounds were treated with a variety of reagents containing hydride

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