(2S,4R)-tert-Butyl 4-(((benzyloxy)carbonyl)amino)-2-(hydroxymethyl)pyrrolidine-1-carboxylate

95%

Reagent Code: #36556
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CAS Number 1194057-63-0

science Other reagents with same CAS 1194057-63-0

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Weight 350.4095 g/mol
Formula C₁₈H₂₆N₂O₅
badge Registry Numbers
MDL Number MFCD18801151
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description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the field of medicinal chemistry. It serves as a key intermediate in the production of pharmaceutical agents, especially those targeting neurological and cardiovascular disorders. Its structure, featuring both a hydroxymethyl group and a protected amine, makes it valuable for constructing peptide-like frameworks and other biologically active compounds. Additionally, it is employed in the development of protease inhibitors and other enzyme-targeting drugs, leveraging its ability to mimic natural substrates. The tert-butyl and benzyloxycarbonyl groups provide stability and selective reactivity, facilitating controlled chemical transformations in multi-step synthetic routes.

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inventory 100mg
10-20 days ฿8,235.00

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(2S,4R)-tert-Butyl 4-(((benzyloxy)carbonyl)amino)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
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This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the field of medicinal chemistry. It serves as a key intermediate in the production of pharmaceutical agents, especially those targeting neurological and cardiovascular disorders. Its structure, featuring both a hydroxymethyl group and a protected amine, makes it valuable for constructing peptide-like frameworks and other biologically active compounds. Additionally, it is employed in the development of proteas
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the field of medicinal chemistry. It serves as a key intermediate in the production of pharmaceutical agents, especially those targeting neurological and cardiovascular disorders. Its structure, featuring both a hydroxymethyl group and a protected amine, makes it valuable for constructing peptide-like frameworks and other biologically active compounds. Additionally, it is employed in the development of protease inhibitors and other enzyme-targeting drugs, leveraging its ability to mimic natural substrates. The tert-butyl and benzyloxycarbonyl groups provide stability and selective reactivity, facilitating controlled chemical transformations in multi-step synthetic routes.
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