1-(tert-butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid

Reagent Code: #39541
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CAS Number 40350-82-1

science Other reagents with same CAS 40350-82-1

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Weight 231.25 g/mol
Formula C₁₀H₁₇NO₅
inventory_2 Storage & Handling
Storage 2-8℃

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This chemical is primarily used in organic synthesis as a protected form of 4-hydroxypyrrolidine-2-carboxylic acid. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of peptide-based drugs and bioactive compounds. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during complex molecular constructions, enhancing the efficiency of multi-step synthesis processes. Additionally, it is employed in the development of chiral catalysts and ligands, which are crucial in asymmetric synthesis for creating enantiomerically pure substances. Its stability and ease of deprotection under mild conditions make it a valuable tool in medicinal chemistry and drug discovery.

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inventory 200mg
10-20 days ฿9,000.00

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1-(tert-butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid
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This chemical is primarily used in organic synthesis as a protected form of 4-hydroxypyrrolidine-2-carboxylic acid. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of peptide-based drugs and bioactive compounds. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during complex molecular constructions, enhancing the efficiency of multi-step synthesis processes. Additionally, it is employed in the development of chiral catalysts an

This chemical is primarily used in organic synthesis as a protected form of 4-hydroxypyrrolidine-2-carboxylic acid. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of peptide-based drugs and bioactive compounds. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during complex molecular constructions, enhancing the efficiency of multi-step synthesis processes. Additionally, it is employed in the development of chiral catalysts and ligands, which are crucial in asymmetric synthesis for creating enantiomerically pure substances. Its stability and ease of deprotection under mild conditions make it a valuable tool in medicinal chemistry and drug discovery.

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