CAS 86042-28-6
:1,5-Di-O-(4-methylbenzoyl)-2,3-O-isopropylidene-beta-D-ribofuranose
Description:
1,5-Di-O-(4-methylbenzoyl)-2,3-O-isopropylidene-beta-D-ribofuranose is a chemical compound that belongs to the class of ribofuranosides, which are derivatives of ribose sugar. This compound features two 4-methylbenzoyl groups attached to the 1 and 5 positions of the ribofuranose ring, providing it with distinctive aromatic characteristics. The isopropylidene group at the 2 and 3 positions serves to protect the hydroxyl groups, enhancing the compound's stability and solubility in organic solvents. The presence of the methyl group on the benzoyl moiety contributes to its lipophilicity, which can influence its biological activity and interactions. This compound is typically used in synthetic organic chemistry, particularly in the synthesis of nucleoside analogs and other biologically relevant molecules. Its structural features suggest potential applications in medicinal chemistry, where modifications to sugar moieties can lead to compounds with improved pharmacological properties. As with many organic compounds, it is essential to handle it with care, following appropriate safety protocols.
Formula:C24H26O7
InChI:InChI=1/C24H26O7/c1-14-5-9-16(10-6-14)21(25)27-13-18-19-20(31-24(3,4)30-19)23(28-18)29-22(26)17-11-7-15(2)8-12-17/h5-12,18-20,23H,13H2,1-4H3/t18-,19-,20-,23+/m1/s1
Synonyms:- 1,5-Di-O-(4-methylbenzoyl)-2,3-O-isopropylidene-β-D- ribofuranose
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Found 2 products.
2,3-O-Isopropylidene-1,5-di-O-toluoyl-b-D-ribofuranose
CAS:<p>2,3-O-Isopropylidene-1,5-di-O-toluoyl-b-D-ribofuranose (IPDT) is a saccharide that is modified with a methyl group at the 2' position of the ribose. This modification can be used to control the rate of glycosylation reactions, or to synthesize oligosaccharides and complex carbohydrates. IPDT is also an important precursor for click chemistry reactions, which are used in the synthesis of polymers and other organic compounds.</p>Formula:C24H26NO7Purity:Min. 95%Molecular weight:440.47 g/mol

