trans-1-(tert-butoxycarbonyl)-4-(2,4-dimethoxyphenyl)pyrrolidine-3-carboxylic acid

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Reagent Code: #241874
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CAS Number 2227659-66-5

science Other reagents with same CAS 2227659-66-5

blur_circular Chemical Specifications

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Weight 351.4 g/mol
Formula C₁₈H₂₅NO₆
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its structure supports the construction of complex pyrrolidine-based scaffolds, which are common in drug discovery for their conformational rigidity and improved metabolic stability. The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective functionalization of the nitrogen atom during multi-step syntheses. The dimethoxyphenyl moiety contributes to aromatic interactions in receptor binding, making this compound valuable in optimizing lead compounds for enhanced affinity and selectivity. Commonly employed in medicinal chemistry research for generating analogs in structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,000.00
inventory 1g
10-20 days ฿17,640.00
inventory 100mg
10-20 days ฿5,040.00

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trans-1-(tert-butoxycarbonyl)-4-(2,4-dimethoxyphenyl)pyrrolidine-3-carboxylic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its structure supports the construction of complex pyrrolidine-based scaffolds, which are common in drug discovery for their conformational rigidity and improved metabolic stability. The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective functionalization of the nitrogen atom during multi-step syntheses. The dimethoxyphenyl moiety contributes to aromatic interactions in receptor binding, making this compound valuable in optimizing lead compounds for enhanced affinity and selectivity. Commonly employed in medicinal chemistry research for generating analogs in structure-activity relationship (SAR) studies.
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