(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyl-3-phenylpropanoic acid
≥95%
- Product Code: 50135
CAS:
152436-04-9
| Molecular Weight: | 401.45 g./mol | Molecular Formula: | C₂₅H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02259493 | |
| Melting Point: | Boiling Point: | 621.2°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. It helps in the selective protection of the amino group during the formation of peptide bonds, ensuring that the reaction proceeds efficiently without unwanted side reactions. The fluorenylmethoxycarbonyl (Fmoc) group, which is part of this compound, is particularly valued for its stability under basic conditions and its ease of removal under mild acidic conditions. This makes it highly suitable for solid-phase peptide synthesis, where it allows for the stepwise assembly of peptides on a resin. Additionally, its chiral structure ensures the correct stereochemistry is maintained during the synthesis process, which is crucial for producing biologically active peptides.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $127.47 |
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| 1.000 | 10-20 days | $319.14 |
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| 5.000 | 10-20 days | $1,177.10 |
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| 10.000 | 10-20 days | $1,963.18 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyl-3-phenylpropanoic acid
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. It helps in the selective protection of the amino group during the formation of peptide bonds, ensuring that the reaction proceeds efficiently without unwanted side reactions. The fluorenylmethoxycarbonyl (Fmoc) group, which is part of this compound, is particularly valued for its stability under basic conditions and its ease of removal under mild acidic conditions. This makes it highly suitable for solid-phase peptide synthesis, where it allows for the stepwise assembly of peptides on a resin. Additionally, its chiral structure ensures the correct stereochemistry is maintained during the synthesis process, which is crucial for producing biologically active peptides.
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