trans-1-(tert-Butoxycarbonyl)-4-(pyridin-3-yl)pyrrolidine-3-carboxylic acid

95%

Reagent Code: #54160
fingerprint
CAS Number 1212132-10-9

science Other reagents with same CAS 1212132-10-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.3300 g/mol
Formula C₁₅H₂₀N₂O₄
badge Registry Numbers
MDL Number MFCD06659319
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those targeting neurological and inflammatory disorders. Its structure, featuring both a pyridine and a pyrrolidine ring, makes it a valuable building block for designing molecules with potential therapeutic effects. Researchers often employ it in the synthesis of small molecule inhibitors or modulators of specific enzymes or receptors. Additionally, its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enhancing its utility in complex drug discovery projects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,470.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
trans-1-(tert-Butoxycarbonyl)-4-(pyridin-3-yl)pyrrolidine-3-carboxylic acid
No image available
This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those targeting neurological and inflammatory disorders. Its structure, featuring both a pyridine and a pyrrolidine ring, makes it a valuable building block for designing molecules with potential therapeutic effects. Researchers often employ it in the synthesis of small molecule inhibitors or modulators of specific enzymes or receptors. Additionally, its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enhancing its utility in complex drug discovery projects.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...