(3S,4R)-1-Cbz-4-methylpyrrolidine-3-carboxylic Acid

≥95%

Reagent Code: #76155
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CAS Number 1428243-71-3

science Other reagents with same CAS 1428243-71-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.29 g/mol
Formula C₁₄H₁₇NO₄
badge Registry Numbers
MDL Number MFCD27991306
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used in pharmaceutical research as a key intermediate for synthesizing complex molecules, particularly in the development of drugs targeting neurological disorders. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are crucial for ensuring drug efficacy and safety. Additionally, it serves as a building block in peptide synthesis, aiding in the production of biologically active peptides. Its protective Cbz group allows for selective reactions, enabling precise modifications in multi-step organic synthesis.

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Test Parameter Specification
APPEARANCE White to yellow solid
Purity 95-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿22,023.00
inventory 250mg
10-20 days ฿8,784.00

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(3S,4R)-1-Cbz-4-methylpyrrolidine-3-carboxylic Acid
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Used in pharmaceutical research as a key intermediate for synthesizing complex molecules, particularly in the development of drugs targeting neurological disorders. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are crucial for ensuring drug efficacy and safety. Additionally, it serves as a building block in peptide synthesis, aiding in the production of biologically active peptides. Its protective Cbz group allows for selective reactions, enabling precise modif

Used in pharmaceutical research as a key intermediate for synthesizing complex molecules, particularly in the development of drugs targeting neurological disorders. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are crucial for ensuring drug efficacy and safety. Additionally, it serves as a building block in peptide synthesis, aiding in the production of biologically active peptides. Its protective Cbz group allows for selective reactions, enabling precise modifications in multi-step organic synthesis.

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