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

95%

Reagent Code: #76147
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CAS Number 1428243-36-0

science Other reagents with same CAS 1428243-36-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.29 g/mol
Formula C₁₄H₁₇NO₄
badge Registry Numbers
MDL Number MFCD27991305
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used in the synthesis of pharmaceutical compounds, particularly in the development of chiral drugs. It serves as a key intermediate in the production of biologically active molecules, including those targeting neurological disorders. Its chiral structure makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure substances. Additionally, it is employed in peptide chemistry for the modification and design of peptide-based therapeutics. Its versatility also extends to research applications in medicinal chemistry, aiding in the exploration of new drug candidates.

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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,600.00
inventory 1g
10-20 days ฿30,105.00

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(3R,4S)-1-Cbz-4-methylpyrrolidine-3-carboxylic Acid
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Used in the synthesis of pharmaceutical compounds, particularly in the development of chiral drugs. It serves as a key intermediate in the production of biologically active molecules, including those targeting neurological disorders. Its chiral structure makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure substances. Additionally, it is employed in peptide chemistry for the modification and design of peptide-based therapeutics. Its versatility also extends to researc

Used in the synthesis of pharmaceutical compounds, particularly in the development of chiral drugs. It serves as a key intermediate in the production of biologically active molecules, including those targeting neurological disorders. Its chiral structure makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure substances. Additionally, it is employed in peptide chemistry for the modification and design of peptide-based therapeutics. Its versatility also extends to research applications in medicinal chemistry, aiding in the exploration of new drug candidates.

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