cis-2-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid

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Reagent Code: #54740
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CAS Number 136315-70-3

science Other reagents with same CAS 136315-70-3

blur_circular Chemical Specifications

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Weight 229.2729 g/mol
Formula C₁₁H₁₉NO₄
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MDL Number MFCD00800539
inventory_2 Storage & Handling
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description Product Description

This chemical is primarily used in the synthesis of peptides and other organic compounds, serving as a protected amino acid derivative. Its structure, featuring a tert-butoxycarbonyl (Boc) group, makes it valuable in peptide chemistry for protecting the amino group during reactions. It is often employed in solid-phase peptide synthesis (SPPS) to build complex peptide chains, ensuring selective deprotection and coupling steps. Additionally, it finds application in the preparation of cyclopentane-based drug candidates, where the cyclopentane ring contributes to the conformational rigidity of the molecule, enhancing its binding affinity to biological targets. Its stability and compatibility with various reaction conditions make it a versatile intermediate in medicinal chemistry and pharmaceutical research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,386.00

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cis-2-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid
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This chemical is primarily used in the synthesis of peptides and other organic compounds, serving as a protected amino acid derivative. Its structure, featuring a tert-butoxycarbonyl (Boc) group, makes it valuable in peptide chemistry for protecting the amino group during reactions. It is often employed in solid-phase peptide synthesis (SPPS) to build complex peptide chains, ensuring selective deprotection and coupling steps. Additionally, it finds application in the preparation of cyclopentane-based dru

This chemical is primarily used in the synthesis of peptides and other organic compounds, serving as a protected amino acid derivative. Its structure, featuring a tert-butoxycarbonyl (Boc) group, makes it valuable in peptide chemistry for protecting the amino group during reactions. It is often employed in solid-phase peptide synthesis (SPPS) to build complex peptide chains, ensuring selective deprotection and coupling steps. Additionally, it finds application in the preparation of cyclopentane-based drug candidates, where the cyclopentane ring contributes to the conformational rigidity of the molecule, enhancing its binding affinity to biological targets. Its stability and compatibility with various reaction conditions make it a versatile intermediate in medicinal chemistry and pharmaceutical research.

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