Structure

Boc-Trp-OH

CAS
13139-14-5
Catalog Number
ACM13139145-1
Category
Amino Acids
Molecular Weight
304.34
Molecular Formula
C16H20N2O4

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Specification

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)

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.

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