Fmoc-6-Ahx-OH

• CAS: 88574-06-5
• Catalog Number: ACM88574065
• Category: Amino Acids
• Molecular Weight: 353.41
• Molecular Formula: C21H23NO4
• Description: Standard building block for introduction of aminohexanoic amino-acid residues by Fmoc SPPS.
• Synonyms: 6-(Fmoc-amino)caproic acid, 6-(Fmoc-amino)hexanoic acid, Fmoc-ε-Ahx-OH, N-ε-Fmoc-ε-aminocaproic acid, Fmoc-6-aminohexanoic acid
• Canonical SMILES: OC(=O)CCCCCNC(=O)OCC1c2ccccc2-c3ccccc13
• InChI: 1S/C21H23NO4/c23-20(24)12-2-1-7-13-22-21(25)26-14-19-17-10-5-3-8-15(17)16-9-4-6-11-18(16)19/h3-6,8-11,19H,1-2,7,12-14H2,(H,22,25)(H,23,24)
• InChI Key: FPCPONSZWYDXRD-UHFFFAOYSA-N
• Application: Peptide synthesis.
• Assay: ≥97.0% (HPLC)
• Beilstein: 5883220
• Color: white
• Form: powder
• Functional Group: Fmoc
• MDL Number: MFCD00077045
• NACRES: NA.26
• PubChem ID: 329747869
• Quality Level: 200
• Reaction Suitability: reaction type: Fmoc solid-phase peptide synthesis
• Storage Temperature: 2-8℃
• Type: Unusual Amino Acids, Aliphatic Amino Acids

Synthetic Use

Upstream Synthesis Route 1

• 82911-69-1
• 60-32-2

• 88574-06-5

Reference: [1] Organic and Biomolecular Chemistry, 2018, vol. 16, # 39, p. 7139 - 7142

Upstream Synthesis Route 2

• 28920-43-6
• 60-32-2

• 88574-06-5

Reference: [1] Russian Journal of Bioorganic Chemistry, 2005, vol. 31, # 4, p. 352 - 356

Upstream Synthesis Route 3

• 102774-86-7
• 60-32-2

• 88574-06-5

Reference: [1] Helvetica Chimica Acta, 2000, vol. 83, # 6, p. 1268 - 1277

Downstream Synthesis Route 1

• 50-00-0
• 88574-06-5

• 173690-47-6

Reference: [1]Russian Journal of Bioorganic Chemistry,2005,vol. 31,p. 352 - 356

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