tert-butyl trans-3-(hydroxymethyl)-4-(4-methoxyphenyl)pyrrolidine-1-carboxylate

90%

Reagent Code: #241885
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CAS Number 1186654-76-1

science Other reagents with same CAS 1186654-76-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.39 g/mol
Formula C₁₇H₂₅NO₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structural features, including the trans-configured pyrrolidine ring and protected hydroxymethyl group, make it valuable in asymmetric synthesis and chiral drug design. Commonly employed in medicinal chemistry for constructing complex targets where stereochemical control is critical. The tert-butyl carbamate (Boc) protection allows for selective deprotection and further functionalization during multi-step syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿6,950.00
1g
10-20 days ฿18,000.00
50mg
10-20 days ฿2,340.00
tert-butyl trans-3-(hydroxymethyl)-4-(4-methoxyphenyl)pyrrolidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structural features, including the trans-configured pyrrolidine ring and protected hydroxymethyl group, make it valuable in asymmetric synthesis and chiral drug design. Commonly employed in medicinal chemistry for constructing complex targets where stereochemical control is critical. The tert-butyl carbamate (Boc) protection allows fo

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structural features, including the trans-configured pyrrolidine ring and protected hydroxymethyl group, make it valuable in asymmetric synthesis and chiral drug design. Commonly employed in medicinal chemistry for constructing complex targets where stereochemical control is critical. The tert-butyl carbamate (Boc) protection allows for selective deprotection and further functionalization during multi-step syntheses.

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