Boc-Pro-OH

• CAS: 15761-39-4
• Catalog Number: ACM15761394
• Category: Amino Acids
• Molecular Weight: 215.25
• Description: Standard building block for introduction of proline amino-acid residues by Boc SPPS.
• Synonyms: Boc-Pro-OH, N-α-t.-Boc-L-proline
• InChI: 1S/C10H17NO4/c1-10(2,3)15-9(14)11-6-4-5-7(11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)
• InChI Key: ZQEBQGAAWMOMAI-UHFFFAOYSA-N
• Application: Peptide synthesis.
• Assay: ≥98% (TLC)
• Form: powder
• Functional Group: Boc
• MDL Number: MFCD00037324
• Quality Level: 200
• Reaction Suitability: reaction type: Boc solid-phase peptide synthesis
• Storage Temperature: 2-30℃

Synthetic Use

Downstream Synthesis Route 1

• 186581-53-3
• 15761-39-4

• 56502-01-3

Reference: [1] Organic Syntheses, 2002, vol. 79, p. 154 - 154

Downstream Synthesis Route 2

• 15761-39-4

• 34381-71-0

Reference: [1] Tetrahedron Letters, 1983, vol. 24, # 33, p. 3513 - 3516

Downstream Synthesis Route 3

• 15761-39-4

• 56502-01-3

Reference: [1] Tetrahedron Letters, 1997, vol. 38, # 20, p. 3609 - 3610
[2] RSC Advances, 2014, vol. 4, # 70, p. 37419 - 37422

Downstream Synthesis Route 4

• 15761-39-4
• 16652-76-9

• 53363-79-4

Reference: [1]Agricultural and Biological Chemistry,1985,vol. 49,p. 2587 - 2596

Downstream Synthesis Route 5

• 15761-39-4
• 34622-39-4
• 25024-53-7

• 57818-01-6

Reference: [1]Journal of Medicinal Chemistry,1981,vol. 24,p. 692 - 698

Downstream Synthesis Route 6

• 15761-39-4
• 53100-44-0
• 177609-24-4

• 24305-27-9

Reference: [1]Journal of the Chemical Society. Perkin transactions I,1996,p. 753 - 754

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