Boc-Trp-OH

• CAS: 13139-14-5
• Catalog Number: ACM13139145-1
• Category: Amino Acids
• Molecular Weight: 304.34
• Molecular Formula: C16H20N2O4
• Description: Building block for introduction of tryptophan amino-acid residues by Boc SPPS.
• Synonyms: Boc-Trp-OH, N-α-t.-Boc-L-tryptophan
• InChI: 1S/C16H20N2O4/c1-16(2,3)22-15(21)18-13(14(19)20)8-10-9-17-12-7-5-4-6-11(10)12/h4-7,9,13,17H,8H2,1-3H3,(H,18,21)(H,19,20)/p-1/t13-/m0/s1
• InChI Key: NFVNYBJCJGKVQK-ZDUSSCGKSA-M
• Application: Peptide synthesis.
• Assay: ≥98% (TLC)
• Form: powder
• Functional Group: Boc
• MDL Number: MFCD00065595
• Quality Level: 200
• Reaction Suitability: reaction type: Boc solid-phase peptide synthesis
• Storage Temperature: 2-30℃
• Type: Unlabeled Standard Amino Acids, Tryptophan (Trp)

Synthetic Use

Downstream Synthesis Route 1

• 53267-93-9
• 13139-14-5

• 37169-36-1

Reference: [1] RSC Advances, 2015, vol. 5, # 74, p. 60354 - 60364

Downstream Synthesis Route 2

• 100-39-0
• 13139-14-5

• 57229-67-1

Reference: [1] Organic and Biomolecular Chemistry, 2013, vol. 11, # 10, p. 1594 - 1597

Downstream Synthesis Route 3

• 13139-14-5

• 5022-65-1

Reference: [1] Patent: WO2018/33724, 2018, A1,

Downstream Synthesis Route 4

• 21715-90-2
• 13139-14-5

• 53666-03-8

Reference: [1]Doklady Chemistry,1994,vol. 337,p. 133 - 135
Doklady Akademii Nauk SSSR,1994,vol. 337,p. 205 - 207

Downstream Synthesis Route 5

• 55661-33-1
• 13139-14-5

• 200864-67-1

Reference: [1]Russian Journal of Bioorganic Chemistry,1995,vol. 21,p. 115 - 120
Bioorganicheskaya Khimiya,1995,vol. 21,p. 133 - 138

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