28810-03-9

Usage

Chemical structure

A complex carbohydrate derivative with multiple acetyl and iodine groups attached to a hexopyranose ring.

Functional groups

Contains acetyl (-COCH3) and iodine (-I) groups, which contribute to its chemical and biological properties.

Solubility

The high level of acetylation may impact the solubility of the compound in various solvents, potentially affecting its reactivity and bioavailability.

Reactivity

The presence of multiple functional groups, such as acetyl and iodine, may influence the reactivity of the molecule in chemical reactions.

Bioavailability

The structure and functional groups of the compound may affect its ability to be absorbed and utilized by living organisms.

Potential applications

Due to its unique structure and properties, the compound may have potential as a pharmaceutical agent, a synthetic intermediate, or a research reagent.

Further study

More research is needed to fully understand the properties and potential uses of 1,2,3-tri-O-acetyl-6-deoxy-6-iodo-4-O-(2,3,4,6-tetra-O-acetylhexopyranosyl)hexopyranose.

Upstream product

• 28810-01-7 1,2,3-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-β-D-glucopyranose 
• 28868-67-9 2,3-di-O-acetyl-1,6-anhydro-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-β-D-glycopyranose 
• 137886-93-2 Acetic acid (2S,3R,4S,5R,6R)-2,3-diacetoxy-6-formyloxymethyl-5-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester 
• 137887-18-4 hexa-O-acetyl-6-O-formylmaltosyl chloride 
• 108-24-7 acetic anhydride 
• 28810-02-8 O¹,O²,O³-triacetyl-O⁴-(tetra-O-acetyl-α-D-glucopyranosyl)-O⁶-(toluene-4-sulfonyl)-β-D-glucopyranose 

Downstream Products

• 28810-04-0 1,2,3-tri-O-acetyl-6-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-β-D-glucopyranose 
• 67831-15-6 Maltose-5-en-heptaacetat 
• 1189789-87-4 C₂₄H₃₂O₁₅ 
• 1189789-86-3 C₂₄H₃₂O₁₅ 

Relevant academic research and scientific papers

Selectively deoxygenated derivatives of β-maltosyl-(1→4)-trehalose as biological probes

The four derivatives of β-maltosyl-(1→4)-trehalose have been synthesized, which are monodeoxygenated at the site of one of the primary hydroxyl groups. The tetrasaccharides were constructed in [2+2] block syntheses. Thus, 6?-deoxy-β-maltosyl-(1→4)-trehalo

Chemoenzymatic Approach to the Preparation of Regioselectively Modified Cyclodextrins. The Substrate Specificity of the Enzyme Cyclodextrin Glucosyltransferase (CGTase)

The synthesis of α-maltosyl fluorides substituted at the 6- or 6'-position with H, F, Br, OMe, OAc is described, together with the preparation of the 4-thio-α-maltosyl fluoride and 5-thio-α-D-glucosyl fluoride.These compounds were obtained by chemical or enzymatic procedures and their structures have been established by 13C NMR spectroscopy.The glycosyl fluorides have been tested as substrates for the enzyme CGTase under coupling and condensation conditions.It has been found that all the compounds tested are substrates in coupling reactions.Only three of them led to higher oligosaccharides with a modified maltosyl residue as repeating unit, but only the 6'-O-Me and 6'-O-acetyl fluorides were transformed into cyclic compounds.Under the conditions used, 6A, 6C, 6E-tri-O-methylcyclomaltohexaose, 6A, 6C, 6E-tri-O-methylcyclomaltoheptaose, and 6A, 6C, 6E, 6G-tetra-O-methylcyclomaltooctaose were isolated in 42, 13 and 16 percent yield, respectively.The 6'-O-acetylmaltosyl fluoride afforded 6A, 6C, 6E-tri-O-acetylcyclomaltohexaose and a mixture of partially acetylated cyclomaltoheptaoses in only low yields. By this approach, new insights have been obtained on the specificity of the catalytic site of CGTase of Bacillus macerans and new route for the preparation of regioselectively modified cyclodextrins have been developed.