(9H-Fluoren-9-yl)methyl 4-hydroxypiperidine-1-carboxylate
97%
- Product Code: 37146
CAS:
351184-42-4
Molecular Weight: | 323.3857 g./mol | Molecular Formula: | C₂₀H₂₁NO₃ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 510.7 °C at 760 mmHg | |
Density: | 1.26g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in peptide chemistry, where it serves as a protecting group for amines. Its fluorenylmethyl (Fmoc) group is widely employed in solid-phase peptide synthesis (SPPS) to temporarily shield amino groups during the stepwise assembly of peptide chains. The Fmoc group can be selectively removed under mild basic conditions, such as with piperidine, without affecting other functional groups in the molecule. This makes it a valuable tool for constructing complex peptides and proteins with high precision. Additionally, its stability under acidic conditions allows for compatibility with various synthetic strategies, enhancing its versatility in chemical research and pharmaceutical development.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿5,229.00 |
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(9H-Fluoren-9-yl)methyl 4-hydroxypiperidine-1-carboxylate
This compound is primarily utilized in organic synthesis, particularly in peptide chemistry, where it serves as a protecting group for amines. Its fluorenylmethyl (Fmoc) group is widely employed in solid-phase peptide synthesis (SPPS) to temporarily shield amino groups during the stepwise assembly of peptide chains. The Fmoc group can be selectively removed under mild basic conditions, such as with piperidine, without affecting other functional groups in the molecule. This makes it a valuable tool for constructing complex peptides and proteins with high precision. Additionally, its stability under acidic conditions allows for compatibility with various synthetic strategies, enhancing its versatility in chemical research and pharmaceutical development.
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