CAS 353754-90-2
:Phenylmethyl 6-deoxy-2,3,4-tris-O-(phenylmethyl)-L-mannopyranoside
Description:
Phenylmethyl 6-deoxy-2,3,4-tris-O-(phenylmethyl)-L-mannopyranoside, with the CAS number 353754-90-2, is a glycoside derivative of L-mannose. This compound features a pyranose ring structure, which is characteristic of many sugars, and is modified with multiple phenylmethyl (benzyl) groups that enhance its hydrophobic properties. The presence of these phenylmethyl groups can influence the compound's solubility, stability, and potential interactions with biological systems. The 6-deoxy modification indicates the absence of a hydroxyl group at the sixth carbon, which can affect the compound's reactivity and biological activity. Such glycosides are often studied for their potential applications in pharmaceuticals, as they may exhibit unique biological activities, including antimicrobial or antitumor properties. The structural complexity and functional groups present in this compound make it a subject of interest in organic synthesis and medicinal chemistry, where modifications can lead to the development of new therapeutic agents.
Formula:C34H36O5
InChI:InChI=1S/C34H36O5/c1-26-31(35-22-27-14-6-2-7-15-27)32(36-23-28-16-8-3-9-17-28)33(37-24-29-18-10-4-11-19-29)34(39-26)38-25-30-20-12-5-13-21-30/h2-21,26,31-34H,22-25H2,1H3/t26-,31-,32+,33+,34?/m0/s1
InChI key:InChIKey=WFDBDGICTJECRL-KJDDAZAPSA-N
SMILES:O(CC1=CC=CC=C1)[C@@H]2[C@H](OCC3=CC=CC=C3)[C@@H](OCC4=CC=CC=C4)[C@H](C)OC2OCC5=CC=CC=C5
Synonyms:- Phenylmethyl 6-deoxy-2,3,4-tris-O-(phenylmethyl)-L-mannopyranoside
- L-Mannopyranoside, phenylmethyl 6-deoxy-2,3,4-tris-O-(phenylmethyl)-
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Found 2 products.
1,2,3,4-Tetra-O-benzyl-L-rhamnopyranoside
CAS:<p>Tetra-O-benzyl-L-rhamnopyranoside is a modification of L-rhamnopyranoside, an oligosaccharide with the formula CHO. It is a complex carbohydrate that can be synthesized from monosaccharides and polysaccharides. Tetra-O-benzyl-L-rhamnopyranoside is a high purity, custom synthesis, and synthetic product. The product is soluble in water and has a sweet taste. Tetra-O-benzyl-L-rhamnopyranoside is used in the synthesis of saccharides, glycosylation, methylation, fluorination, and click chemistry reactions.</p>Formula:C34H36O5Purity:Min. 95%Molecular weight:524.65 g/mol

