Di-tert-butyl (R)-2-(aminomethyl)piperazine-1,4-dicarboxylate

97%

Reagent Code: #37514
fingerprint
CAS Number 1932411-32-9

science Other reagents with same CAS 1932411-32-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.4085 g/mol
Formula C₁₅H₂₉N₃O₄
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of chiral intermediates for pharmaceutical applications. It serves as a key building block in the development of active pharmaceutical ingredients (APIs), particularly in the creation of drugs targeting neurological and cardiovascular disorders. Its chiral nature allows for the production of enantiomerically pure compounds, which is crucial for ensuring the efficacy and safety of the final drug product. Additionally, it is employed in organic synthesis for the preparation of complex molecules, where its tert-butyl groups provide steric protection during reactions, enhancing selectivity and yield.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,600.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Di-tert-butyl (R)-2-(aminomethyl)piperazine-1,4-dicarboxylate
No image available

This compound is primarily utilized in the synthesis of chiral intermediates for pharmaceutical applications. It serves as a key building block in the development of active pharmaceutical ingredients (APIs), particularly in the creation of drugs targeting neurological and cardiovascular disorders. Its chiral nature allows for the production of enantiomerically pure compounds, which is crucial for ensuring the efficacy and safety of the final drug product. Additionally, it is employed in organic synthesis

This compound is primarily utilized in the synthesis of chiral intermediates for pharmaceutical applications. It serves as a key building block in the development of active pharmaceutical ingredients (APIs), particularly in the creation of drugs targeting neurological and cardiovascular disorders. Its chiral nature allows for the production of enantiomerically pure compounds, which is crucial for ensuring the efficacy and safety of the final drug product. Additionally, it is employed in organic synthesis for the preparation of complex molecules, where its tert-butyl groups provide steric protection during reactions, enhancing selectivity and yield.

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...