(R)-1-Benzyl 2-methyl piperazine-1,2-dicarboxylate

95%

Reagent Code: #230153
fingerprint
CAS Number 1217598-28-1

science Other reagents with same CAS 1217598-28-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.3 g/mol
Formula C₁₄H₁₈N₂O₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a chiral building block for developing drugs targeting central nervous system disorders due to the presence of the piperazine ring, which is common in neuroactive molecules. Its ester groups allow for further chemical modifications, enabling the creation of diverse compound libraries for drug discovery. Also utilized in asymmetric synthesis where the R-configuration plays a role in achieving desired stereochemistry in final products.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,470.00
inventory 250mg
10-20 days ฿4,440.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-1-Benzyl 2-methyl piperazine-1,2-dicarboxylate
No image available

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a chiral building block for developing drugs targeting central nervous system disorders due to the presence of the piperazine ring, which is common in neuroactive molecules. Its ester groups allow for further chemical modifications, enabling the creation of diverse compound libraries for drug discovery. Also utilized in asymmetric synthesis where the R-configuration plays a rol

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a chiral building block for developing drugs targeting central nervous system disorders due to the presence of the piperazine ring, which is common in neuroactive molecules. Its ester groups allow for further chemical modifications, enabling the creation of diverse compound libraries for drug discovery. Also utilized in asymmetric synthesis where the R-configuration plays a role in achieving desired stereochemistry in final products.

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...