(S)-1-(tert-Butoxycarbonyl)-2-(4-iodobenzyl)pyrrolidine-2-carboxylic acid

≥95%

Reagent Code: #51355
fingerprint
CAS Number 1217686-40-2

science Other reagents with same CAS 1217686-40-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 431.27 g/mol
Formula C₁₇H₂₂INO₄
badge Registry Numbers
MDL Number MFCD06796820
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its structure, featuring a pyrrolidine ring and an iodobenzyl group, makes it valuable for constructing molecules with specific stereochemistry and functional groups. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthetic processes. Additionally, the iodine atom provides a handle for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. Its applications are particularly relevant in the development of peptidomimetics and other small molecules targeting therapeutic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,451.00
inventory 1g
10-20 days ฿37,080.00
inventory 250mg
10-20 days ฿14,796.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-1-(tert-Butoxycarbonyl)-2-(4-iodobenzyl)pyrrolidine-2-carboxylic acid
No image available

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its structure, featuring a pyrrolidine ring and an iodobenzyl group, makes it valuable for constructing molecules with specific stereochemistry and functional groups. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivi

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its structure, featuring a pyrrolidine ring and an iodobenzyl group, makes it valuable for constructing molecules with specific stereochemistry and functional groups. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthetic processes. Additionally, the iodine atom provides a handle for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. Its applications are particularly relevant in the development of peptidomimetics and other small molecules targeting therapeutic pathways.

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...