1-Pyrrolidinecarboxylic acid, 3-methylene-, phenylmethyl ester

98%

Reagent Code: #223305
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CAS Number 150543-35-4

science Other reagents with same CAS 150543-35-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.2637 g/mol
Formula C₁₃H₁₅NO₂
badge Registry Numbers
MDL Number MFCD14582417
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It serves as a building block for the preparation of various bioactive molecules and drug candidates. Its structure allows for the introduction of pyrrolidine motifs, which are commonly found in medicinal compounds due to their favorable pharmacokinetic properties. Commonly employed in the synthesis of protease inhibitors and other enzyme modulators. Also utilized in research settings for developing novel heterocyclic compounds. The benzyloxycarbonyl (Cbz) protecting group safeguards the pyrrolidine nitrogen, enabling selective reactions at other functional sites, such as the exocyclic methylene group, during multi-step syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,200.00
inventory 1g
10-20 days ฿6,400.00
inventory 5g
10-20 days ฿19,200.00
1-Pyrrolidinecarboxylic acid, 3-methylene-, phenylmethyl ester
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It serves as a building block for the preparation of various bioactive molecules and drug candidates. Its structure allows for the introduction of pyrrolidine motifs, which are commonly found in medicinal compounds due to their favorable pharmacokinetic properties. Commonly employed in the synthesis of protease inhibitors and other enzyme modulators. Also utilized in research settings for developing novel hete
Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It serves as a building block for the preparation of various bioactive molecules and drug candidates. Its structure allows for the introduction of pyrrolidine motifs, which are commonly found in medicinal compounds due to their favorable pharmacokinetic properties. Commonly employed in the synthesis of protease inhibitors and other enzyme modulators. Also utilized in research settings for developing novel heterocyclic compounds. The benzyloxycarbonyl (Cbz) protecting group safeguards the pyrrolidine nitrogen, enabling selective reactions at other functional sites, such as the exocyclic methylene group, during multi-step syntheses.
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