1-Cyclopentyl-L-Proline Methyl Ester

98%

Reagent Code: #165643
fingerprint
CAS Number 1485728-95-7

science Other reagents with same CAS 1485728-95-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.27 g/mol
Formula C₁₁H₁₉NO₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in pharmaceutical research as a chiral building block for the synthesis of biologically active compounds. Its structure combines a proline scaffold with a cyclopentyl group, making it valuable in the development of enzyme inhibitors and receptor modulators. Commonly employed in medicinal chemistry for optimizing peptide-based drugs, particularly those targeting central nervous system disorders and metabolic diseases. Also utilized in asymmetric synthesis due to its stereochemical stability and ability to direct selective reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,110.00
inventory 250mg
10-20 days ฿13,500.00
inventory 1g
10-20 days ฿22,730.00
inventory 5g
10-20 days ฿67,910.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Cyclopentyl-L-Proline Methyl Ester
No image available

Used in pharmaceutical research as a chiral building block for the synthesis of biologically active compounds. Its structure combines a proline scaffold with a cyclopentyl group, making it valuable in the development of enzyme inhibitors and receptor modulators. Commonly employed in medicinal chemistry for optimizing peptide-based drugs, particularly those targeting central nervous system disorders and metabolic diseases. Also utilized in asymmetric synthesis due to its stereochemical stability and abili

Used in pharmaceutical research as a chiral building block for the synthesis of biologically active compounds. Its structure combines a proline scaffold with a cyclopentyl group, making it valuable in the development of enzyme inhibitors and receptor modulators. Commonly employed in medicinal chemistry for optimizing peptide-based drugs, particularly those targeting central nervous system disorders and metabolic diseases. Also utilized in asymmetric synthesis due to its stereochemical stability and ability to direct selective reactions.

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...