Boc-Asp(OBzl)-OH

• CAS: 7536-58-5
• Catalog Number: ACM7536585
• Category: Amino Acids
• Molecular Weight: 323.34
• Description: Building block for introduction of aspartic acid amino-acid residues by Boc SPPS.
• Synonyms: Boc-Asp(OBzl)-OH, N-α-t.-Boc-L-aspartic acid β-benzyl ester
• InChI: 1S/C16H21NO6/c1-16(2,3)23-15(21)17-12(14(19)20)9-13(18)22-10-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,19,20)
• InChI Key: SOHLZANWVLCPHK-UHFFFAOYSA-N
• Application: Peptide synthesis.
• Assay: ≥98% (TLC)
• Form: powder
• Functional Group: carboxylic acid
• MDL Number: MFCD00065564
• Quality Level: 200
• Reaction Suitability: reaction type: Boc solid-phase peptide synthesis
• Storage Temperature: 2-30℃

Synthetic Use

Upstream Synthesis Route 1

• 24424-99-5
• 2177-63-1

• 7536-58-5

Reference: [1] Patent: CN106866502, 2017, A, . Location in patent: Paragraph 0230-0234

Upstream Synthesis Route 2

• 18595-34-1
• 2177-63-1

• 7536-58-5

Reference: [1]Justus Liebigs Annalen der Chemie,1968,vol. 716,p. 175 - 185

Downstream Synthesis Route 1

• 7536-58-5

• 13726-67-5

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

Downstream Synthesis Route 2

• 7536-58-5

• 2177-63-1

Reference: [1] Journal of the American Chemical Society, 1995, vol. 117, # 17, p. 4729 - 4741
[2] Tetrahedron, 2016, vol. 72, # 13, p. 1706 - 1715

Downstream Synthesis Route 3

• 7536-58-5

• 13726-67-5

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

Downstream Synthesis Route 4

• 21715-90-2
• 7536-58-5

• 66851-88-5

Reference: [1]Current Patent Assignee: FEDERAL STATE UNITARY ENTERPRISE OF RUSSIAN FEDERATION - EP2397488, 2019, B1
Location in patent: Paragraph 0171; 0172

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