2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-methylpentanoicacid

97%

  • Product Code: 197461
  CAS:    2250198-69-5
Molecular Weight: 353.41 g./mol Molecular Formula: C₂₁H₂₃NO₄
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature
Product Description: Widely used in peptide synthesis as a protected amino acid derivative, this compound enables selective coupling reactions by shielding the amine group with the Fmoc (fluorenylmethyloxycarbonyl) protecting group. Its primary application is in solid-phase peptide synthesis (SPPS), where it allows stepwise assembly of peptides under mild basic conditions. The Fmoc group can be easily removed using piperidine, leaving other protecting groups intact, which makes it ideal for synthesizing complex polypeptides with high purity. It is especially useful in the production of pharmaceutical peptides, research reagents, and in the development of peptide-based drugs. The steric bulk of the fluorenyl group also helps minimize side reactions during coupling, improving yield and efficiency.
Sizes / Availability / Pricing:
Size Availability Price Quantity
250mg 10-20 days ฿10,730.00
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-
1g 10-20 days ฿19,300.00
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-
5g 10-20 days ฿61,400.00
+
-
100mg 10-20 days ฿5,750.00
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-
2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-methylpentanoicacid
Widely used in peptide synthesis as a protected amino acid derivative, this compound enables selective coupling reactions by shielding the amine group with the Fmoc (fluorenylmethyloxycarbonyl) protecting group. Its primary application is in solid-phase peptide synthesis (SPPS), where it allows stepwise assembly of peptides under mild basic conditions. The Fmoc group can be easily removed using piperidine, leaving other protecting groups intact, which makes it ideal for synthesizing complex polypeptides with high purity. It is especially useful in the production of pharmaceutical peptides, research reagents, and in the development of peptide-based drugs. The steric bulk of the fluorenyl group also helps minimize side reactions during coupling, improving yield and efficiency.
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