tert-Butyl2-acetylpyrrolidine-1-carboxylate

98%

Reagent Code: #155639
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CAS Number 92012-22-1

science Other reagents with same CAS 92012-22-1

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Weight 213.27 g/mol
Formula C₁₁H₁₉NO₃
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MDL Number MFCD16308624
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Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected form of acetylpyrrolidine, allowing selective reactions at other functional sites without interference. Commonly employed in the development of bioactive molecules, including neurologically active agents and enzyme inhibitors. Its tert-butoxycarbonyl (Boc) protection group enables easy deprotection under mild acidic conditions, making it valuable in multi-step synthesis. Also utilized in medicinal chemistry for constructing peptidomimetics and other nitrogen-containing heterocycles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,350.00
inventory 250mg
10-20 days ฿3,920.00
inventory 1g
10-20 days ฿9,530.00
inventory 5g
10-20 days ฿35,060.00

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tert-Butyl2-acetylpyrrolidine-1-carboxylate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected form of acetylpyrrolidine, allowing selective reactions at other functional sites without interference. Commonly employed in the development of bioactive molecules, including neurologically active agents and enzyme inhibitors. Its tert-butoxycarbonyl (Boc) protection group enables easy deprotection under mild acidic conditions, making it valuable in multi-step synthesis. Als

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected form of acetylpyrrolidine, allowing selective reactions at other functional sites without interference. Commonly employed in the development of bioactive molecules, including neurologically active agents and enzyme inhibitors. Its tert-butoxycarbonyl (Boc) protection group enables easy deprotection under mild acidic conditions, making it valuable in multi-step synthesis. Also utilized in medicinal chemistry for constructing peptidomimetics and other nitrogen-containing heterocycles.

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