(R)-(9H-Fluoren-9-yl)methyl (1-hydroxy-3-methylbutan-2-yl)carbamate

97%

  • Product Code: 37297
  CAS:    215178-46-4
Molecular Weight: 325.40 g./mol Molecular Formula: C₂₀H₂₃NO₃
EC Number: MDL Number: MFCD00270229
Melting Point: Boiling Point: 515.7±33.0°C at 760 mmHg
Density: Storage Condition: 2-8°C, dry and sealed
Product Description: This compound is primarily utilized in the field of organic synthesis, particularly in peptide chemistry. It serves as a protective group for amines during the synthesis of peptides, ensuring selective reactions at specific sites without unwanted side reactions. Its fluorenylmethyl moiety allows for easy removal under mild conditions, making it a valuable tool in the stepwise construction of complex peptide structures. Additionally, its chiral nature can be leveraged in asymmetric synthesis to induce stereoselectivity in the formation of target molecules. Its application extends to the development of pharmaceuticals and bioactive compounds where precise control over molecular structure is critical.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days €9.26
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0.250 10-20 days €15.43
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1.000 10-20 days €46.78
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(R)-(9H-Fluoren-9-yl)methyl (1-hydroxy-3-methylbutan-2-yl)carbamate
This compound is primarily utilized in the field of organic synthesis, particularly in peptide chemistry. It serves as a protective group for amines during the synthesis of peptides, ensuring selective reactions at specific sites without unwanted side reactions. Its fluorenylmethyl moiety allows for easy removal under mild conditions, making it a valuable tool in the stepwise construction of complex peptide structures. Additionally, its chiral nature can be leveraged in asymmetric synthesis to induce stereoselectivity in the formation of target molecules. Its application extends to the development of pharmaceuticals and bioactive compounds where precise control over molecular structure is critical.
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