(2S,5S)-1-(tert-Butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic acid

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Reagent Code: #36593
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CAS Number 334769-80-1

science Other reagents with same CAS 334769-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.27 g/mol
Formula C₁₁H₁₉NO₄
badge Registry Numbers
MDL Number MFCD13185989
thermostat Physical Properties
Boiling Point 343.2±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. Its role as a protected amino acid derivative makes it valuable in solid-phase peptide synthesis (SPPS), where it helps in constructing complex peptide chains with high precision. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during the synthesis process, preventing unwanted side reactions. Additionally, it is employed in the production of chiral intermediates for active pharmaceutical ingredients (APIs), contributing to the creation of enantiomerically pure compounds. Its application extends to research and development in medicinal chemistry, where it aids in exploring new therapeutic agents and optimizing drug efficacy.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿13,716.00
inventory 10g
10-20 days ฿20,592.00
inventory 1g
10-20 days ฿4,446.00
inventory 250mg
10-20 days ฿1,782.00

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(2S,5S)-1-(tert-Butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic acid
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This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. Its role as a protected amino acid derivative makes it valuable in solid-phase peptide synthesis (SPPS), where it helps in constructing complex peptide chains with high precision. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during the synthesis process, preventing unwanted side reactions. Additionally, it is employed in the production of chiral in

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. Its role as a protected amino acid derivative makes it valuable in solid-phase peptide synthesis (SPPS), where it helps in constructing complex peptide chains with high precision. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during the synthesis process, preventing unwanted side reactions. Additionally, it is employed in the production of chiral intermediates for active pharmaceutical ingredients (APIs), contributing to the creation of enantiomerically pure compounds. Its application extends to research and development in medicinal chemistry, where it aids in exploring new therapeutic agents and optimizing drug efficacy.

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