(1S,4S)-4-[[(1,1-Dimethylethoxy)Carbonyl]Amino]-2-Cyclopentene-1-Carboxylic Acid

98%

Reagent Code: #237352
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CAS Number 1329035-82-6

science Other reagents with same CAS 1329035-82-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.26 g/mol
Formula C₁₁H₁₇NO₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like structures where stereochemical control is critical. Commonly employed in medicinal chemistry for constructing constrained ring systems that mimic peptide bonds, enhancing metabolic stability and target selectivity. Also utilized in asymmetric synthesis and as an intermediate in the preparation of cyclic amino acid derivatives.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,440.00
inventory 1g
10-20 days ฿46,950.00
inventory 5g
10-20 days ฿164,860.00
inventory 250mg
10-20 days ฿16,860.00
(1S,4S)-4-[[(1,1-Dimethylethoxy)Carbonyl]Amino]-2-Cyclopentene-1-Carboxylic Acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like structures where stereochemical control is critical. Commonly employed in medicinal chemistry for constructing constrained ring systems that mimic peptide bonds, enhancing metabolic stability and target selectivity. Also utilized in asymmetric synthesis and as an i

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like structures where stereochemical control is critical. Commonly employed in medicinal chemistry for constructing constrained ring systems that mimic peptide bonds, enhancing metabolic stability and target selectivity. Also utilized in asymmetric synthesis and as an intermediate in the preparation of cyclic amino acid derivatives.

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