N-Fmoc-D-Valine
98%
- Product Code: 105050
Alias:
Fmoc-D-valine ; Fmoc-D-valine
CAS:
84624-17-9
Molecular Weight: | 339.39 g./mol | Molecular Formula: | C₂₀H₂₁NO₄ |
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EC Number: | MDL Number: | MFCD00062953 | |
Melting Point: | 143-144 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
N-Fmoc-D-Valine is widely used in peptide synthesis as a building block. It serves as a protected form of D-valine, where the Fmoc group acts as a temporary protecting group for the amino group during the synthesis process. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), enabling the stepwise construction of peptides with high precision. Its application ensures the selective deprotection of the amino group, allowing for the sequential addition of amino acids to form complex peptide chains. Additionally, it is employed in the preparation of chiral compounds and in research involving unnatural amino acids, contributing to advancements in biochemistry, medicinal chemistry, and drug development.
Product Specification:
Test | Specification |
---|---|
Melting Point | 144-148 |
Purity (GC) | 98-100% |
Specific Rotation [A]20/D(C=1, DMF) | 15-19 |
Appearance | White To Light Yellow Powder |
Infrared Spectrometry | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿270.00 |
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5.000 | 10-20 days | ฿350.00 |
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25.000 | 10-20 days | ฿890.00 |
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100.000 | 10-20 days | ฿3,530.00 |
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500.000 | 10-20 days | ฿15,460.00 |
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N-Fmoc-D-Valine
N-Fmoc-D-Valine is widely used in peptide synthesis as a building block. It serves as a protected form of D-valine, where the Fmoc group acts as a temporary protecting group for the amino group during the synthesis process. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), enabling the stepwise construction of peptides with high precision. Its application ensures the selective deprotection of the amino group, allowing for the sequential addition of amino acids to form complex peptide chains. Additionally, it is employed in the preparation of chiral compounds and in research involving unnatural amino acids, contributing to advancements in biochemistry, medicinal chemistry, and drug development.
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