Boc-His-OH

• CAS: 17791-52-5
• Catalog Number: ACM17791525
• Category: Amino Acids
• Molecular Weight: 255.27
• Description: Building block for introduction of histidine amino-acid residues by Boc SPPS.
• Synonyms: Boc-His-OH, N-α-t.-Boc-L-histidine
• InChI: 1S/C11H17N3O4/c1-11(2,3)18-10(17)14-8(9(15)16)4-7-5-12-6-13-7/h5-6,8H,4H2,1-3H3,(H,12,13)(H,14,17)(H,15,16)/p-1/t8-/m0/s1
• InChI Key: AYMLQYFMYHISQO-QMMMGPOBSA-M
• Application: Peptide synthesis.
• Assay: ≥98% (TLC)
• Form: powder
• Functional Group: Boc
• MDL Number: MFCD00065576
• Quality Level: 200
• Reaction Suitability: reaction type: Boc solid-phase peptide synthesis
• Storage Temperature: 2-30℃

Synthetic Use

Upstream Synthesis Route 1

• 83468-83-1

• 17791-52-5

Reference: [1] Tetrahedron Letters, 2002, vol. 43, # 2, p. 311 - 313

Upstream Synthesis Route 2

• 5934-29-2
• 58632-95-4

• 17791-52-5

Reference: [1]Kawasaki; Miyano; Murakami; Kakimi
[Chemical and Pharmaceutical Bulletin, 1989, vol. 37, # 11, p. 3112 - 3113]

Downstream Synthesis Route 1

• 596-43-0
• 17791-52-5

• 32926-43-5

Reference: [1] Chemistry of Natural Compounds, 1982, vol. 18, # 3, p. 322 - 327[2] Khimiya Prirodnykh Soedinenii, 1982, # 3, p. 349 - 354

Downstream Synthesis Route 2

• 17791-52-5

• 32926-43-5

Reference: [1] Chemistry of Natural Compounds, 1982, vol. 18, # 3, p. 322 - 327[2] Khimiya Prirodnykh Soedinenii, 1982, # 3, p. 349 - 354

Downstream Synthesis Route 3

• 98-59-9
• 17791-52-5

• 35899-43-5

Reference: [1]Journal of Medicinal Chemistry,1993,vol. 36,p. 2431 - 2447

Downstream Synthesis Route 4

• 596-43-0
• 17791-52-5

• 32926-43-5

Reference: [1]Chemistry of Natural Compounds,1982,vol. 18,p. 322 - 327
Khimiya Prirodnykh Soedinenii,1982,p. 349 - 354

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