Fmoc-Gly-OH

• CAS: 29022-11-5
• Catalog Number: ACM29022115
• Category: Amino Acids
• Molecular Weight: 297.31
• Molecular Formula: C17H15NO4
• Description: High purity Fmoc-protected amino acid for research and process production of peptides, with very low levels of dipeptide, free-amino acids and acetic acid impurities.; Standard building block for introduction of glycine amino-acid residues by Fmoc SPPS.
• Synonyms: Fmoc-Gly-OH, FMOC-Glycine, N-α-Fmoc-glycine
• InChI: 1S/C17H15NO4/c19-16(20)9-18-17(21)22-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15H,9-10H2,(H,18,21)(H,19,20)
• InChI Key: NDKDFTQNXLHCGO-UHFFFAOYSA-N
• Melting Point: 177.4℃
• Application: Peptide synthesis.
• Assay: ≥98% (TLC); ≥98.0% (acidimetric); ≥99.0% (HPLC)
• Form: powder
• Functional Group: Fmoc
• MDL Number: MFCD00037140
• Quality Level: 400
• Reaction Suitability: reaction type: Fmoc solid-phase peptide synthesis
• Storage Temperature: 2-30℃
• Type: Unlabeled Standard Amino Acids, Glycine (Gly)

Synthetic Use

Upstream Synthesis Route 1

• 1227363-07-6
• 28920-43-6

• 29022-11-5
• 35661-60-0
• 35661-39-3
• 35661-38-2
• 135248-89-4

Reference: [1] Journal of Physical Chemistry B, 2010, vol. 114, # 19, p. 6751 - 6762

Downstream Synthesis Route 1

• 29022-11-5
• 71989-26-9
• 109425-51-6

• 49557-75-7

Reference: [1] Dalton Transactions, 2005, # 4, p. 728 - 734

Downstream Synthesis Route 2

• 29022-11-5
• 100-52-7

• 17360-47-3

Reference: [1] Tetrahedron Letters, 1996, vol. 37, # 27, p. 4819 - 4822

* For details of the synthesis route, please refer to the original source to ensure accuracy.