
Catalog Number	AR003OV4
Chemical Name	Beta-D-Ribofuranose 1,2,3,5-tetraacetate
CAS Number	13035-61-5
Molecular Formula	C13H18O9
Molecular Weight	318.2766
MDL Number	MFCD00005358
SMILES	CC(=O)OC[C@H]1O[C@H]([C@@H]([C@@H]1OC(=O)C)OC(=O)C)OC(=O)C

Beta-D-Ribofuranose 1,2,3,5-tetraacetate, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure containing acetyl groups on multiple positions enables it to participate in various reactions to form complex molecules. In organic chemistry, $name$ is commonly used as a protective group for the hydroxyl groups in the ribose moiety. By selectively deprotecting these acetyl groups at specific stages of a synthesis sequence, chemists can control the regioselectivity and stereochemistry of subsequent reactions.Moreover, $name$ serves as a key intermediate in the synthesis of nucleoside analogs and other bioactive compounds. Its stability under mild conditions allows for manipulation without disturbing the delicate sugar backbone, making it an ideal candidate for constructing pharmaceutical agents and nucleic acid derivatives. Through strategic deprotection and functional group interconversions, chemists can access a vast array of potentially valuable molecules for medicinal and material applications.In summary, the strategic use of Beta-D-Ribofuranose 1,2,3,5-tetraacetate in chemical synthesis enables precise control over the modification of biomolecules and the construction of structurally diverse compounds with tailored properties, thus expanding the possibilities for innovative drug discovery and materials development.

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(3R,4S,5R,6R)-6-(Acetoxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate

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1,2,3,4-TETRA-O-ACETYL-ALPHA-D-ARABINOPYRANOSE

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GHS Pictogram
Signal Word	Warning
UN#	N/A
Hazard Statements	H315-H319-H335
Precautionary Statements	P261-P305+P351+P338
Class	N/A
Packing Group	N/A

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