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Methyl 4-O-acetyl-3-O-benzyl-2,6-dideoxy-α-D-lyxo-hexopyranoside is a complex organic compound with the molecular formula C16H20O6. It is a derivative of a hexopyranoside, which is a type of sugar molecule. The compound features a methyl group attached to the 4th carbon, an acetyl group (an ester of acetic acid) at the 4th oxygen, and a benzyl group (a phenylmethyl group) at the 3rd oxygen. The 2nd and 6th carbons are dideoxy, meaning they lack two hydroxyl groups typically found in hexopyranosides. methyl 4-O-acetyl-3-O-benzyl-2,6-dideoxy-α-D-lyxo-hexopyranoside is significant in organic chemistry and biochemistry, particularly in the synthesis of complex carbohydrates and as a building block for various pharmaceuticals and natural product derivatives. Its structure and functional groups make it a versatile intermediate in chemical synthesis, allowing for further modification and application in a range of scientific and industrial processes.

4833-12-9

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4833-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4833-12-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4833-12:
(6*4)+(5*8)+(4*3)+(3*3)+(2*1)+(1*2)=89
89 % 10 = 9
So 4833-12-9 is a valid CAS Registry Number.

4833-12-9Relevant academic research and scientific papers

Investigation of Different Synthetic Approaches towards Methyl 2,6-Dideoxy-α-D-arabino- and -α-D-lyxo-hexopyranosides

Kjoelberg, Ove,Neumann, Klaus

, p. 721 - 727 (2007/10/02)

New synthetic routes for making available different methyl 2,6-dideoxyhexopyranosides are reported.Starting with methyl 6-deoxy-2,3-O-isopropylidene-α-D-manno- and -α-D-talo-pyranoside the respective methyl 2,6-dideoxy-α-D-arabino- and α-D-lyxo-hexopyrano

A Highly Stereoselective Synthesis of the AB Disaccharide Unit of Olivomycin A

Roush, William R.,Lin, Xiaofa,Straub, Julie A.

, p. 1649 - 1655 (2007/10/02)

A highly stereoselective synthesis of the AB disaccharide (4c) of olivomycin A is described.The synthesis features the double asymmetric allylboration of α,β-dialkoxy aldehyde 8 using tartrate allylboronate (S,S)-9, which provides triol derivative 10 with

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