(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxy-3-methylbutanoic acid

97%

  • Product Code: 37755
  CAS:    884880-39-1
Molecular Weight: 355.38 g./mol Molecular Formula: C₂₀H₂₁NO₅
EC Number: MDL Number: MFCD02682577
Melting Point: Boiling Point: 595.5±50.0°C at 760 mmHg
Density: Storage Condition: 2-8°C, dry and sealed
Product Description: This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group during the synthesis process, allowing selective reactions to occur at other functional groups. The hydroxyl and carboxyl groups in the molecule can also be utilized for further chemical modifications or conjugation. Its application is particularly significant in solid-phase peptide synthesis (SPPS), where it ensures the stepwise assembly of peptides with high precision. Additionally, its chiral nature makes it valuable in the synthesis of enantiomerically pure compounds, which are essential in pharmaceutical research and development.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days Ft43,150.30
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0.250 10-20 days Ft86,203.64
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxy-3-methylbutanoic acid
This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group during the synthesis process, allowing selective reactions to occur at other functional groups. The hydroxyl and carboxyl groups in the molecule can also be utilized for further chemical modifications or conjugation. Its application is particularly significant in solid-phase peptide synthesis (SPPS), where it ensures the stepwise assembly of peptides with high precision. Additionally, its chiral nature makes it valuable in the synthesis of enantiomerically pure compounds, which are essential in pharmaceutical research and development.
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