N-Boc-4-(Fmoc-amino)piperidine-4-carboxylic acid

97%

Reagent Code: #65722
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CAS Number 183673-66-7

science Other reagents with same CAS 183673-66-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 466.53 g/mol
Formula C₂₆H₃₀N₂O₆
badge Registry Numbers
MDL Number MFCD01318741
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This compound is primarily used in peptide synthesis as a building block. It serves as a protected intermediate, where the Boc (tert-butoxycarbonyl) and Fmoc (fluorenylmethyloxycarbonyl) groups protect the amine functionalities. This allows for selective deprotection and coupling during solid-phase peptide synthesis, enabling the construction of complex peptide structures. It is particularly useful in the synthesis of peptides containing piperidine moieties, which are common in bioactive molecules. Its dual protection strategy ensures precise control over the sequence and structure of the synthesized peptides, making it valuable in pharmaceutical research and drug development.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Off-White Powder or Crystals
Purity 97-100
Oxygen (Elemental Analysis) 19.8-20.8
Infrared Spectrum Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿2,170.00
500mg
10-20 days ฿1,280.00
5g
10-20 days ฿8,820.00
25g
10-20 days ฿30,320.00
N-Boc-4-(Fmoc-amino)piperidine-4-carboxylic acid
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This compound is primarily used in peptide synthesis as a building block. It serves as a protected intermediate, where the Boc (tert-butoxycarbonyl) and Fmoc (fluorenylmethyloxycarbonyl) groups protect the amine functionalities. This allows for selective deprotection and coupling during solid-phase peptide synthesis, enabling the construction of complex peptide structures. It is particularly useful in the synthesis of peptides containing piperidine moieties, which are common in bioactive molecules. Its d

This compound is primarily used in peptide synthesis as a building block. It serves as a protected intermediate, where the Boc (tert-butoxycarbonyl) and Fmoc (fluorenylmethyloxycarbonyl) groups protect the amine functionalities. This allows for selective deprotection and coupling during solid-phase peptide synthesis, enabling the construction of complex peptide structures. It is particularly useful in the synthesis of peptides containing piperidine moieties, which are common in bioactive molecules. Its dual protection strategy ensures precise control over the sequence and structure of the synthesized peptides, making it valuable in pharmaceutical research and drug development.

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