Methyl 1-Boc-2-pyrrolidinecarboxylate

98%

  • Product Code: 173382
  CAS:    145681-01-2
Molecular Weight: 229.27 g./mol Molecular Formula: C₁₁H₁₉NO₄
EC Number: MDL Number: MFCD03762834
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, dry
Product Description: Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds containing pyrrolidine scaffolds. Its protected amine group allows for selective reactions at other functional sites, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors, cognitive enhancers, and central nervous system agents. The ester functionality can be hydrolyzed to the corresponding carboxylic acid for further derivatization, enabling incorporation into peptides or complex heterocycles. Widely utilized in medicinal chemistry for structure-activity relationship studies due to its conformational rigidity and chiral stability.
Product Specification:
Test Specification
Appearance Colorless to light yellow liquid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size Availability Price Quantity
1g 10-20 days ฿180.00
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5g 10-20 days ฿390.00
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25g 10-20 days ฿1,880.00
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100g 10-20 days ฿5,880.00
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500g 10-20 days ฿25,500.00
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Methyl 1-Boc-2-pyrrolidinecarboxylate
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds containing pyrrolidine scaffolds. Its protected amine group allows for selective reactions at other functional sites, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors, cognitive enhancers, and central nervous system agents. The ester functionality can be hydrolyzed to the corresponding carboxylic acid for further derivatization, enabling incorporation into peptides or complex heterocycles. Widely utilized in medicinal chemistry for structure-activity relationship studies due to its conformational rigidity and chiral stability.
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