5,8,11,14,17,20,23,26-Octaoxa-2-azanonacosanedioic acid 1-(9H-fluoren-9-ylmethyl) ester
98%
- Product Code: 63580
CAS:
756526-02-0
| Molecular Weight: | 663.76 g./mol | Molecular Formula: | C₃₄H₄₉NO₁₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Seal |
Product Description:
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protective group for carboxylic acids. The fluorenylmethyl ester (Fm ester) group is particularly effective in preventing unwanted side reactions during the synthesis process. It is commonly employed in solid-phase peptide synthesis (SPPS) to protect the carboxyl terminus of amino acids, ensuring the selective formation of peptide bonds. The compound’s stability under basic conditions and its ability to be removed under mild acidic conditions make it a valuable tool in the production of complex peptides and proteins. Additionally, its application extends to the preparation of peptide-based pharmaceuticals and bioactive molecules, where precise control over chemical reactions is critical.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to yellow liquid |
| PURITY | 97.5 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,250.00 |
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| 0.250 | 10-20 days | ฿2,830.00 |
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| 1.000 | 10-20 days | ฿10,950.00 |
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5,8,11,14,17,20,23,26-Octaoxa-2-azanonacosanedioic acid 1-(9H-fluoren-9-ylmethyl) ester
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protective group for carboxylic acids. The fluorenylmethyl ester (Fm ester) group is particularly effective in preventing unwanted side reactions during the synthesis process. It is commonly employed in solid-phase peptide synthesis (SPPS) to protect the carboxyl terminus of amino acids, ensuring the selective formation of peptide bonds. The compound’s stability under basic conditions and its ability to be removed under mild acidic conditions make it a valuable tool in the production of complex peptides and proteins. Additionally, its application extends to the preparation of peptide-based pharmaceuticals and bioactive molecules, where precise control over chemical reactions is critical.
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