Fmoc-Thr[GalNAc(Ac)3-α-D]-OH

• CAS: 116783-35-8
• Catalog Number: ACM116783358-1
• Category: Amino Acids
• Molecular Weight: 670.66
• Description: The O-glycosidic linkage and the O-acetyl protection in this building block is 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-O-β-(2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-galactopyranosyl)-L-threonine
• Canonical SMILES: CC(N[C@@H]1[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H](COC(C)=O)O[C@@H]1O[C@H](C)[C@H](NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O)C(O)=O)=O
• InChI: 1S/C33H38N2O13/c1-16(27(31(40)41)35-33(42)44-14-25-23-12-8-6-10-21(23)22-11-7-9-13-24(22)25)45-32-28(34-17(2)36)30(47-20(5)39)29(46-19(4)38)26(48-32)15-43-18(3)37/h6-13,16,25-30,32H,14-15H2,1-5H3,(H,34,36)(H,35,42)(H,40,41)/t16-,26-,27+,28-,29+,30-,32+/m1/s1
• InChI Key: OXLCJWGAUPPZQJ-ZNHCDWFHSA-N
• Melting Point: 178-183℃
• Application: Peptide synthesis.
• Assay: 0.97
• Form: solid
• Functional Group: Fmoc
• MDL Number: MFCD00171374
• Optical Activity: [α]22/D +55.0°, c = 1% in chloroform
• PubChem ID: 329767565
• Quality Level: 100
• Reaction Suitability: reaction type: Fmoc solid-phase peptide synthesis
• Storage Temperature: -20℃