3-(((Benzyloxy)carbonyl)amino)bicyclo[1.1.1]pentane-1-carboxylic acid

97%

Reagent Code: #153008
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CAS Number 1935125-14-6

science Other reagents with same CAS 1935125-14-6

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key building block in medicinal chemistry, particularly in the synthesis of bioactive molecules and drug candidates. Its rigid bicyclopentane core serves as a bioisostere for phenyl or other aromatic rings, improving metabolic stability and solubility in pharmaceuticals. The carboxylic acid and Cbz-protected amine functionalities allow for straightforward coupling and deprotection steps, making it valuable in peptide-like scaffold construction. Commonly employed in the development of protease inhibitors, kinase inhibitors, and other small-molecule therapeutics where enhanced physicochemical properties are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,870.00
inventory 250mg
10-20 days ฿2,240.00

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3-(((Benzyloxy)carbonyl)amino)bicyclo[1.1.1]pentane-1-carboxylic acid
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Used as a key building block in medicinal chemistry, particularly in the synthesis of bioactive molecules and drug candidates. Its rigid bicyclopentane core serves as a bioisostere for phenyl or other aromatic rings, improving metabolic stability and solubility in pharmaceuticals. The carboxylic acid and Cbz-protected amine functionalities allow for straightforward coupling and deprotection steps, making it valuable in peptide-like scaffold construction. Commonly employed in the development of protease i

Used as a key building block in medicinal chemistry, particularly in the synthesis of bioactive molecules and drug candidates. Its rigid bicyclopentane core serves as a bioisostere for phenyl or other aromatic rings, improving metabolic stability and solubility in pharmaceuticals. The carboxylic acid and Cbz-protected amine functionalities allow for straightforward coupling and deprotection steps, making it valuable in peptide-like scaffold construction. Commonly employed in the development of protease inhibitors, kinase inhibitors, and other small-molecule therapeutics where enhanced physicochemical properties are required.

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