(E)-5-(2,3-bis(tert-butoxycarbonyl)guanidino)pentanoic acid

95%

Reagent Code: #86739
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CAS Number 212567-95-8

science Other reagents with same CAS 212567-95-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 359.42 g/mol
Formula C₁₆H₂₉N₃O₆
badge Registry Numbers
MDL Number MFCD26940326
inventory_2 Storage & Handling
Density 1.15±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily used in the synthesis of peptides and peptidomimetics, particularly in the preparation of arginine analogs. It serves as a protected guanidino building block, enabling the introduction of guanidine functionality into peptide chains while preventing unwanted side reactions during synthesis. The tert-butoxycarbonyl (Boc) groups provide stability under various reaction conditions, making it a valuable intermediate in solid-phase peptide synthesis. Additionally, it is utilized in the development of biologically active compounds, such as enzyme inhibitors and receptor ligands, where the guanidine moiety plays a critical role in binding interactions. Its application extends to medicinal chemistry, where it aids in the design of drug candidates targeting diseases like cancer, cardiovascular disorders, and infectious diseases.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿12,168.00
250mg
10-20 days ฿20,070.00
1g
10-20 days ฿32,760.00
(E)-5-(2,3-bis(tert-butoxycarbonyl)guanidino)pentanoic acid
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This chemical is primarily used in the synthesis of peptides and peptidomimetics, particularly in the preparation of arginine analogs. It serves as a protected guanidino building block, enabling the introduction of guanidine functionality into peptide chains while preventing unwanted side reactions during synthesis. The tert-butoxycarbonyl (Boc) groups provide stability under various reaction conditions, making it a valuable intermediate in solid-phase peptide synthesis. Additionally, it is utilized in t

This chemical is primarily used in the synthesis of peptides and peptidomimetics, particularly in the preparation of arginine analogs. It serves as a protected guanidino building block, enabling the introduction of guanidine functionality into peptide chains while preventing unwanted side reactions during synthesis. The tert-butoxycarbonyl (Boc) groups provide stability under various reaction conditions, making it a valuable intermediate in solid-phase peptide synthesis. Additionally, it is utilized in the development of biologically active compounds, such as enzyme inhibitors and receptor ligands, where the guanidine moiety plays a critical role in binding interactions. Its application extends to medicinal chemistry, where it aids in the design of drug candidates targeting diseases like cancer, cardiovascular disorders, and infectious diseases.

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