CAS 97614-42-1
:α-D-Ribofuranose, 1,3,5-tribenzoate 2-(1H-imidazole-1-sulfonate)
Description:
α-D-Ribofuranose, 1,3,5-tribenzoate 2-(1H-imidazole-1-sulfonate) is a complex organic compound characterized by its structural components, which include a ribofuranose sugar moiety esterified with three benzoate groups and a sulfonate group derived from imidazole. This compound features a ribose sugar in its furanose form, which is a five-membered ring structure, contributing to its biological relevance, particularly in nucleic acid chemistry. The presence of multiple benzoate groups indicates a degree of hydrophobicity, which can influence its solubility and interaction with biological membranes. The imidazole sulfonate moiety may impart unique properties, such as potential buffering capacity or interaction with metal ions, enhancing its utility in biochemical applications. Overall, this compound's structural complexity suggests potential roles in medicinal chemistry, particularly in drug design or as a biochemical probe, due to its ability to interact with various biological targets.
Formula:C29H24N2O10S
InChI:InChI=1S/C29H24N2O10S/c32-26(20-10-4-1-5-11-20)37-18-23-24(39-27(33)21-12-6-2-7-13-21)25(41-42(35,36)31-17-16-30-19-31)29(38-23)40-28(34)22-14-8-3-9-15-22/h1-17,19,23-25,29H,18H2/t23-,24-,25-,29-/m1/s1
InChI key:InChIKey=DHQMZEQWPVIFFR-DOUCHOMGSA-N
SMILES:O(S(=O)(=O)N1C=CN=C1)[C@@H]2[C@H](OC(=O)C3=CC=CC=C3)[C@@H](COC(=O)C4=CC=CC=C4)O[C@@H]2OC(=O)C5=CC=CC=C5
Synonyms:- 2-(1'-Imidazoylsulfonyl)-1,2,5-tri-O-benzoyl-α-D-ribofuranose
- 2-O-(1H-imidazol-1-ylsulfonyl)-1,3,5-tris-O-(phenylcarbonyl)pentofuranose
- α-<span class="text-smallcaps">D</span>-Ribofuranose, 1,3,5-tribenzoate 2-(1H-imidazole-1-sulfonate)
- α-D-Ribofuranose, 1,3,5-tribenzoate 2-(1H-imidazole-1-sulfonate)
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Found 3 products.
1,3,5-Tri-O-benzoyl-2-O-(1H-imidazole-1-sulfonate)-a-D-ribofuranose
CAS:<p>1,3,5-Tri-O-benzoyl-2-O-(1H-imidazole-1-sulfonate)-a-D-ribofuranose (TBIR) is a fatty acid that is synthesized by the condensation of 1,3,5-triacetylbenzene with 2,4,6,-trichlorobenzoyl chloride in the presence of triethylamine and sodium methoxide. TBIR has been shown to be suitable for fabricating polyesters and polyamides. TBIR also has the ability to modify membranes. This modification occurs when TBIR reacts with phospholipids in the membrane bilayer by inserting itself into the membrane bilayer. The mesoporous nature of TBIR allows for diffusional transport through its pores as well as an increased surface area for reactions. It also has a large diameter and branched chains that make it suitable for</p>Formula:C29H24N2O10SPurity:Min. 95%Color and Shape:White PowderMolecular weight:592.57 g/mol
