Rel-(2R,3R)-1-(tert-Butoxycarbonyl)-3-cyclohexylpyrrolidine-2-carboxylic acid

95%

Reagent Code: #54875
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CAS Number 1449586-26-8

science Other reagents with same CAS 1449586-26-8

blur_circular Chemical Specifications

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Weight 297.39 g/mol
Formula C₁₆H₂₇NO₄
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description Product Description

This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic compounds, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a cyclohexyl moiety, makes it valuable for constructing peptidomimetics and other biologically active molecules. The compound is often employed in peptide coupling reactions, where its carboxylic acid group facilitates the formation of amide bonds, essential for creating peptide-based therapeutics. Additionally, its stereochemistry is crucial for ensuring the desired biological activity of the final drug product, making it a critical component in enantioselective synthesis processes.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,874.00
inventory 1mg
10-20 days ฿3,186.00
inventory 25mg
10-20 days ฿29,592.00

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Rel-(2R,3R)-1-(tert-Butoxycarbonyl)-3-cyclohexylpyrrolidine-2-carboxylic acid
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This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic compounds, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a cyclohexyl moiety, makes it valuable for constructing peptidomimetics and other biologically active molecules. The compound is often employed in peptide coupling reactions, where its carboxylic acid grou

This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic compounds, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a cyclohexyl moiety, makes it valuable for constructing peptidomimetics and other biologically active molecules. The compound is often employed in peptide coupling reactions, where its carboxylic acid group facilitates the formation of amide bonds, essential for creating peptide-based therapeutics. Additionally, its stereochemistry is crucial for ensuring the desired biological activity of the final drug product, making it a critical component in enantioselective synthesis processes.

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