(2S,4R)-1-(tert-Butoxycarbonyl)-4-(4-methylbenzyl)pyrrolidine-2-carboxylic acid

≥95%

Reagent Code: #36551
fingerprint
CAS Number 959581-21-6

science Other reagents with same CAS 959581-21-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.40 g/mol
Formula C₁₈H₂₅NO₄
badge Registry Numbers
MDL Number MFCD06659409
thermostat Physical Properties
Boiling Point 461.8±38.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of peptide-based drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a pyrrolidine core, makes it valuable in peptide coupling reactions, where it helps in the controlled assembly of amino acids. The 4-methylbenzyl moiety enhances its stability and reactivity in organic synthesis. It is also employed in the development of protease inhibitors and other bioactive molecules, contributing to advancements in medicinal chemistry and drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,094.00

Cart

No products

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

This compound is primarily used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of peptide-based drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a pyrrolidine core, makes it valuable in peptide coupling reactions, where it helps in the controlled assembly of amino acids. The 4-methylbenzyl moiety enhances its stability and reactivity in organic synthesis. It is also employed in the development of protease inhibitors and other bioacti

This compound is primarily used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of peptide-based drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a pyrrolidine core, makes it valuable in peptide coupling reactions, where it helps in the controlled assembly of amino acids. The 4-methylbenzyl moiety enhances its stability and reactivity in organic synthesis. It is also employed in the development of protease inhibitors and other bioactive molecules, contributing to advancements in medicinal chemistry and drug discovery.

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...