(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(naphthalen-1-yl)propanoic acid
98%
- Product Code: 60686
CAS:
507472-10-8
Molecular Weight: | 437.49 g./mol | Molecular Formula: | C₂₈H₂₃NO₄ |
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EC Number: | MDL Number: | MFCD03427990 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the synthesis process, preventing unwanted reactions. It is particularly useful in solid-phase peptide synthesis (SPPS), where it allows for the stepwise addition of amino acids to build peptides. The naphthalene moiety enhances the stability and solubility of the compound, making it easier to handle in organic solvents. After the peptide chain is assembled, the Fmoc group can be removed under mild basic conditions, ensuring the integrity of the peptide structure. This compound is valuable in producing peptides for pharmaceutical research, drug development, and biochemical studies.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿3,222.00 |
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0.250 | 10-20 days | ฿4,824.00 |
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1.000 | 10-20 days | ฿12,096.00 |
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(naphthalen-1-yl)propanoic acid
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the synthesis process, preventing unwanted reactions. It is particularly useful in solid-phase peptide synthesis (SPPS), where it allows for the stepwise addition of amino acids to build peptides. The naphthalene moiety enhances the stability and solubility of the compound, making it easier to handle in organic solvents. After the peptide chain is assembled, the Fmoc group can be removed under mild basic conditions, ensuring the integrity of the peptide structure. This compound is valuable in producing peptides for pharmaceutical research, drug development, and biochemical studies.
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