(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-phenylpropanoic acid
95%
- Product Code: 38364
CAS:
1217663-60-9
| Molecular Weight: | 387.4279 g./mol | Molecular Formula: | C₂₄H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12198213 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used in peptide synthesis as a protecting group for amino acids. Its fluorenylmethoxycarbonyl (Fmoc) group is particularly valuable in solid-phase peptide synthesis, where it protects the amino group during the coupling of amino acids. The Fmoc group can be easily removed under mild basic conditions, allowing for the sequential assembly of peptides without disrupting the growing chain. This makes it a critical component in the production of peptides for pharmaceutical research, drug development, and biochemical studies. Additionally, its stability and selective deprotection properties make it a preferred choice in organic synthesis and the preparation of complex biomolecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,362.00 |
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-phenylpropanoic acid
This chemical is widely used in peptide synthesis as a protecting group for amino acids. Its fluorenylmethoxycarbonyl (Fmoc) group is particularly valuable in solid-phase peptide synthesis, where it protects the amino group during the coupling of amino acids. The Fmoc group can be easily removed under mild basic conditions, allowing for the sequential assembly of peptides without disrupting the growing chain. This makes it a critical component in the production of peptides for pharmaceutical research, drug development, and biochemical studies. Additionally, its stability and selective deprotection properties make it a preferred choice in organic synthesis and the preparation of complex biomolecules.
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