Fmoc-Trp-OH

• CAS: 35737-15-6
• Catalog Number: ACM35737156
• Category: Amino Acids
• Molecular Weight: 426.46
• Description: Building block for introduction of typtophan by Fmoc SPPS. Superceded by Fmoc-Trp(Boc)-OH.
• Synonyms: Fmoc-Trp-OH, N-α-Fmoc-L-tryptophan
• InChI: 1S/C26H22N2O4/c29-25(30)24(13-16-14-27-23-12-6-5-7-17(16)23)28-26(31)32-15-22-20-10-3-1-8-18(20)19-9-2-4-11-21(19)22/h1-12,14,22,24,27H,13,15H2,(H,28,31)(H,29,30)/p-1/t24-/m0/s1
• InChI Key: MGHMWKZOLAAOTD-DEOSSOPVSA-M
• Application: Peptide synthesis.
• Assay: ≥96.0% (acidimetric); ≥98% (TLC); ≥98.0% (HPLC)
• Form: powder
• Functional Group: Fmoc
• MDL Number: MFCD00037126
• Quality Level: 200
• Reaction Suitability: reaction type: Fmoc solid-phase peptide synthesis
• Storage Temperature: 2-30℃

Synthetic Use

Upstream Synthesis Route 1

• 28920-43-6
• 73-22-3

• 35737-15-6

Reference: [1] Carbohydrate Research, 2006, vol. 341, # 3, p. 322 - 331
[2] Journal of the Chinese Chemical Society, 2011, vol. 58, # 4, p. 509 - 515

Upstream Synthesis Route 2

• 82911-69-1
• 73-22-3

• 35737-15-6

Reference: [1] Russian Journal of Bioorganic Chemistry, 1999, vol. 25, # 5, p. 283 - 287[2] Bioorganicheskaya Khimiya, 1999, vol. 25, # 5, p. 323 - 328
[3] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1995, # 4, p. 723 - 730

Downstream Synthesis Route 1

• 35737-15-6
• 64-19-7

• 1218-34-4

Reference: [1] Asian Journal of Chemistry, 2014, vol. 26, # 10, p. 2941 - 2944

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