Tert-Butyl 3-(Thiophen-2-Yl)Pyrrolidine-1-Carboxylate

95%

Reagent Code: #242799
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CAS Number 630121-93-6

science Other reagents with same CAS 630121-93-6

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scatter_plot Molecular Information
Weight 253.36 g/mol
Formula C₁₃H₁₉NO₂S
badge Registry Numbers
MDL Number MFCD24467030
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of selective receptor modulators due to the presence of a thiophene ring and a functionalized pyrrolidine core. Commonly employed in medicinal chemistry for constructing complex molecules with improved metabolic stability and binding affinity. Also utilized in the preparation of protease inhibitors and cognitive enhancers. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection during multi-step syntheses, making it valuable in drug discovery and development.

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inventory 100mg
10-20 days $914.53

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Tert-Butyl 3-(Thiophen-2-Yl)Pyrrolidine-1-Carboxylate
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of selective receptor modulators due to the presence of a thiophene ring and a functionalized pyrrolidine core. Commonly employed in medicinal chemistry for constructing complex molecules with improved metabolic stability and binding affinity. Also utilized in the preparation of protease inhibitors and cognitive en

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of selective receptor modulators due to the presence of a thiophene ring and a functionalized pyrrolidine core. Commonly employed in medicinal chemistry for constructing complex molecules with improved metabolic stability and binding affinity. Also utilized in the preparation of protease inhibitors and cognitive enhancers. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection during multi-step syntheses, making it valuable in drug discovery and development.

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