Boc-D-Pro-OH

• CAS: 37784-17-1
• Catalog Number: ACM37784171
• Category: Amino Acids
• Molecular Weight: 215.25
• Description: Standard building block for introduction of D-proline amino-acid residues by Boc SPPS.
• Synonyms: Boc-D-Pro-OH, N-α-t.-Boc-D-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
• Melting Point: >132℃
• Application: Peptide synthesis.
• Assay: ≥98% (TLC)
• Form: powder
• Functional Group: Boc
• MDL Number: MFCD00063226
• Quality Level: 200
• Reaction Suitability: reaction type: Boc solid-phase peptide synthesis
• Storage Temperature: 2-30℃

Synthetic Use

Upstream Synthesis Route 1

• 73365-02-3

• 37784-17-1

Reference: [1]Journal of Organic Chemistry,1980,vol. 45,p. 2145 - 2151

Downstream Synthesis Route 1

• 37784-17-1

• 73365-02-3

Reference: [1] Organic Letters, 2006, vol. 8, # 23, p. 5357 - 5360

Downstream Synthesis Route 2

• 37784-17-1
• 74-88-4

• 73323-65-6

Reference: [1] Patent: WO2013/131018, 2013, A1, . Location in patent: Page/Page column 38

Downstream Synthesis Route 3

• 37784-17-1
• 77-78-1

• 73323-65-6

Reference: [1] Journal of Organic Chemistry, 1999, vol. 64, # 21, p. 8014 - 8017

Downstream Synthesis Route 4

• 186581-53-3
• 37784-17-1

• 73323-65-6

Reference: [1]Journal of Organic Chemistry,1980,vol. 45,p. 2145 - 2151

Downstream Synthesis Route 5

• 3339-44-4
• 37784-17-1

• 157016-28-9

Reference: [1]Journal of Organic Chemistry,1994,vol. 59,p. 2437 - 2446
[2]Chemical Communications,2008,p. 4174 - 4176

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