tert-butyl trans-3-(hydroxymethyl)-4-(2-(trifluoromethyl)phenyl)pyrrolidine-1-carboxylate

98%

Reagent Code: #241910
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CAS Number 1186647-92-6

science Other reagents with same CAS 1186647-92-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 345.36 g/mol
Formula C₁₇H₂₂F₃NO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of bioactive molecules targeting central nervous system disorders. Its structural features, including the trifluoromethylphenyl group and protected hydroxymethyl functionality, make it valuable in medicinal chemistry for constructing complex pyrrolidine-based scaffolds. The tert-butyl carbamate (Boc) group allows for selective deprotection and further functionalization, enabling stepwise assembly of drug candidates. Commonly employed in research settings for optimizing potency, selectivity, and metabolic stability in small molecule therapeutics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,220.00
inventory 1g
10-20 days ฿36,870.00
inventory 100mg
10-20 days ฿8,640.00

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tert-butyl trans-3-(hydroxymethyl)-4-(2-(trifluoromethyl)phenyl)pyrrolidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of bioactive molecules targeting central nervous system disorders. Its structural features, including the trifluoromethylphenyl group and protected hydroxymethyl functionality, make it valuable in medicinal chemistry for constructing complex pyrrolidine-based scaffolds. The tert-butyl carbamate (Boc) group allows for selective deprotection and further functionalization, enabling stepwise assembly of drug

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of bioactive molecules targeting central nervous system disorders. Its structural features, including the trifluoromethylphenyl group and protected hydroxymethyl functionality, make it valuable in medicinal chemistry for constructing complex pyrrolidine-based scaffolds. The tert-butyl carbamate (Boc) group allows for selective deprotection and further functionalization, enabling stepwise assembly of drug candidates. Commonly employed in research settings for optimizing potency, selectivity, and metabolic stability in small molecule therapeutics.

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