CAS 289697-66-1
:(5S)-3-methylidene-5-[(1S,2S,3R,4R)-1,2,3,4,5-pentahydroxypentyl]dihydrofuran-2(3H)-one (non-preferred name)
Description:
The chemical substance known as (5S)-3-methylidene-5-[(1S,2S,3R,4R)-1,2,3,4,5-pentahydroxypentyl]dihydrofuran-2(3H)-one, with the CAS number 289697-66-1, is a complex organic compound characterized by its unique structural features. It contains a furan ring, which is a five-membered aromatic ring with oxygen, and exhibits a dihydrofuran-2(3H)-one moiety, indicating the presence of a lactone functional group. The compound also features a chiral center, contributing to its stereochemistry, which is significant in determining its biological activity and interactions. The presence of multiple hydroxyl groups suggests it may exhibit strong hydrogen bonding capabilities, influencing its solubility and reactivity. This compound may be of interest in various fields, including medicinal chemistry and natural product synthesis, due to its potential biological activities and structural complexity. Its specific applications and properties would depend on further studies and characterization, particularly in relation to its stereochemistry and functional groups.
Formula:C10H16O7
InChI:InChI=1/C10H16O7/c1-4-2-6(17-10(4)16)8(14)9(15)7(13)5(12)3-11/h5-9,11-15H,1-3H2/t5-,6+,7-,8-,9+/m1/s1
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Found 4 products.
D-glycero-D-galacto-Nononic acid, 2,3-dideoxy-2-methylene-, γ-lactone (9CI)
CAS:Formula:C10H16O7Color and Shape:SolidMolecular weight:248.22982,3-Dideoxy-2-methylene-D-glycero-D-galacto-nononic Acid γ-Lactone
CAS:Controlled Product<p>Applications Intermediate for the synthesis of KDN and other sialic acids.<br>References Nadano, D., et al.: J. Biol. Chem., 261, 11550 (1986), Livingston, B., et al.: J. Biol. Chem. 263, 9443 (1988).<br></p>Formula:C10H16O7Color and Shape:NeatMolecular weight:248.232,3-Dideoxy-2-methylene-D-glycero-D-galacto-nononic acid γ-lactone
CAS:<p>Methyl 2,3-dideoxy-2-methylene-D-glycero-D-galacto-nononic acid gamma-lactone is a fluorinated derivative of 2,3-dideoxygalactonojirimycin. It is an analog of the natural product 2,3-dideoxygalactonojirimycin and has been shown to inhibit the synthesis of glycolipids in Mycobacterium tuberculosis. Methyl 2,3-dideoxy-2-methylene-D-glycero-D-galacto nononic acid gamma lactone was synthesized by modification of the galactonojirimycin core with methylation at C2 and C3 followed by fluorination at C1.</p>Formula:C10H16O7Purity:Min. 95%Molecular weight:248.23 g/mol




