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CAS 172939-67-2

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3-O-Benzoyl-N-acetyl-a-D-galactosaminyl-1-O-N-(Fmoc)serine Phenacylester

Description:
3-O-Benzoyl-N-acetyl-α-D-galactosaminyl-1-O-N-(Fmoc)serine phenacyl ester is a complex organic compound that features a combination of functional groups, making it significant in biochemical applications, particularly in glycosylation and peptide synthesis. The presence of the benzoyl and phenacyl ester groups indicates that it has potential for use in protecting group strategies during organic synthesis. The N-acetyl-α-D-galactosamine moiety suggests that this compound may play a role in carbohydrate chemistry, particularly in the study of glycoproteins or glycolipids. The Fmoc (9-fluorenylmethoxycarbonyl) group is commonly used as a protective group for amines in peptide synthesis, allowing for selective deprotection under mild conditions. Overall, this compound's structure suggests it may be utilized in the synthesis of glycopeptides or other bioactive molecules, contributing to research in medicinal chemistry and biochemistry. Its specific properties, such as solubility and reactivity, would depend on the surrounding conditions and the presence of other reagents.
Formula:C41H40N2O12
InChI:InChI=1/C41H40N2O12/c1-24(45)42-35-37(55-38(48)26-14-6-3-7-15-26)36(47)34(20-44)54-40(35)52-22-32(39(49)51-23-33(46)25-12-4-2-5-13-25)43-41(50)53-21-31-29-18-10-8-16-27(29)28-17-9-11-19-30(28)31/h2-19,31-32,34-37,40,44,47H,20-23H2,1H3,(H,42,45)(H,43,50)/t32-,34?,35?,36-,37?,40-/m0/s1
SMILES:CC(=NC1C([C@H](C(CO)O[C@@H]1OC[C@@H](C(=O)OCC(=O)c1ccccc1)N=C(O)OCC1c2ccccc2c2ccccc12)O)OC(=O)c1ccccc1)O
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