Fmoc-Ser(Ac3AcNH-ß-Glc)-OH

• CAS: 160067-63-0
• Catalog Number: ACM160067630
• Category: Amino Acids
• Molecular Weight: 656.63
• Molecular Formula: C32H36N2O13
• Description: The O-glycosidic linkage and the O-acetyl protection in this building block are stable to both piperidine and TFA, making it completely compatible with standard protocols in Fmoc solid phase peptide synthesis. Removal of the acetyl-protecting groups is best carried out by treatment of the peptidyl resin with methanolic ammonia prior to cleavage.
• Synonyms: Fmoc-Ser(Ac3AcNH-ß-Glc)-OH, N-α-Fmoc-O-(2-Acetamido-2-deoxy-tri-O-acetyl-β-D-glucopyranosyl)-L-serine
• InChI: 1S/C32H36N2O13/c1-16(35)33-27-29(46-19(4)38)28(45-18(3)37)26(15-42-17(2)36)47-31(27)43-14-25(30(39)40)34-32(41)44-13-24-22-11-7-5-9-20(22)21-10-6-8-12-23(21)24/h5-12,24-29,31H,13-15H2,1-4H3,(H,33,35)(H,34,41)(H,39,40)/t25-,26+,27+,28+,29+,31+/m0/s1
• InChI Key: ORICVOOXZDVFIP-ILRBKQRBSA-N
• Application: Peptide synthesis.
• Assay: ≥97% (TLC); ≥97.0% (HPLC)
• Form: powder
• Functional Group: Fmoc
• Quality Level: 200
• Reaction Suitability: reaction type: Fmoc solid-phase peptide synthesis
• Storage Temperature: 15-25℃
• Type: Unusual Amino Acids, Glycosylated