Boc-D-Phe-OH

• CAS: 18942-49-9
• Catalog Number: ACM18942499
• Category: Amino Acids
• Molecular Weight: 265.3
• Description: Standard building block for introduction of D-phenylalanine amino-acid residues by Boc SPPS.
• Synonyms: Boc-D-Phe-OH, N-α-t.-Boc-D-phenylalanine
• InChI: 1S/C14H19NO4/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,15,18)(H,16,17)/p-1/t11-/m1/s1
• InChI Key: ZYJPUMXJBDHSIF-LLVKDONJSA-M
• Application: Peptide synthesis.
• Assay: ≥98% (TLC); ≥98.0% (HPLC)
• Form: powder
• Functional Group: Boc
• MDL Number: MFCD00063149
• Quality Level: 200
• Reaction Suitability: reaction type: Boc solid-phase peptide synthesis
• Storage Temperature: 2-30℃

Synthetic Use

Downstream Synthesis Route 1

• 67-56-1
• 18942-49-9

• 13033-84-6

Reference: [1] Journal of Organic Chemistry, 1999, vol. 64, # 25, p. 9294 - 9296

Downstream Synthesis Route 2

• 18942-49-9

• 77119-85-8

Reference: [1] Journal of Medicinal Chemistry, 1994, vol. 37, # 18, p. 2918 - 2929

Downstream Synthesis Route 3

• 18942-49-9
• 1117-97-1

• 77119-85-8

Reference: [1] Journal of Peptide Science, 2018, vol. 24, # 3,

Downstream Synthesis Route 4

• 18942-49-9
• 29390-67-8

• 122855-45-2

Reference: [1]Tetrahedron Asymmetry,1990,vol. 1,p. 367 - 370

Downstream Synthesis Route 5

• 18942-49-9
• 18650-39-0

• 172422-78-5

Reference: [1]Tetrahedron,1995,vol. 51,p. 11235 - 11250

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