(2S,4R)-1-(tert-Butoxycarbonyl)-4-(3-chlorobenzyl)pyrrolidine-2-carboxylic acid

≥95%

Reagent Code: #86421
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CAS Number 959576-36-4

science Other reagents with same CAS 959576-36-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 339.81 g/mol
Formula C₁₇H₂₂ClNO₄
badge Registry Numbers
MDL Number MFCD06659395
thermostat Physical Properties
Boiling Point 472.4±35.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in the pharmaceutical and chemical research fields. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a stereospecific (2S,4R)-pyrrolidine ring protected with a tert-butoxycarbonyl (Boc) group, a 3-chlorobenzyl substituent at position 4, and a carboxylic acid at position 2, makes it a valuable building block for creating compounds with potential therapeutic effects. Researchers often employ it in the preparation of peptide analogs and enzyme inhibitors, where its stereochemistry and functional groups play a critical role in enhancing binding affinity and selectivity. Additionally, it is used in medicinal chemistry studies to explore structure-activity relationships and optimize drug candidates for improved efficacy and safety.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,180.00

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(2S,4R)-1-(tert-Butoxycarbonyl)-4-(3-chlorobenzyl)pyrrolidine-2-carboxylic acid
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This compound is primarily utilized in the pharmaceutical and chemical research fields. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a stereospecific (2S,4R)-pyrrolidine ring protected with a tert-butoxycarbonyl (Boc) group, a 3-chlorobenzyl substituent at position 4, and a carboxylic acid at position 2, makes it a valuable building block for

This compound is primarily utilized in the pharmaceutical and chemical research fields. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a stereospecific (2S,4R)-pyrrolidine ring protected with a tert-butoxycarbonyl (Boc) group, a 3-chlorobenzyl substituent at position 4, and a carboxylic acid at position 2, makes it a valuable building block for creating compounds with potential therapeutic effects. Researchers often employ it in the preparation of peptide analogs and enzyme inhibitors, where its stereochemistry and functional groups play a critical role in enhancing binding affinity and selectivity. Additionally, it is used in medicinal chemistry studies to explore structure-activity relationships and optimize drug candidates for improved efficacy and safety.

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