3-(Methylamino)oxetane-3-carboxylicacid

97%

Reagent Code: #213654
fingerprint
CAS Number 1541289-37-5

science Other reagents with same CAS 1541289-37-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 131.13 g/mol
Formula C₅H₉NO₃
badge Registry Numbers
MDL Number MFCD23918087
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of antiviral and antidiabetic drugs, particularly in the development of β-lactamase inhibitors and glucokinase activators. Its strained oxetane ring enhances metabolic stability and improves pharmacokinetic properties in drug candidates. Commonly employed in medicinal chemistry to increase solubility and binding affinity in small molecule therapeutics. Also utilized in the preparation of prodrugs due to its favorable polarity and hydrogen bonding capacity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,700.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-(Methylamino)oxetane-3-carboxylicacid
No image available

Used as a key intermediate in the synthesis of antiviral and antidiabetic drugs, particularly in the development of β-lactamase inhibitors and glucokinase activators. Its strained oxetane ring enhances metabolic stability and improves pharmacokinetic properties in drug candidates. Commonly employed in medicinal chemistry to increase solubility and binding affinity in small molecule therapeutics. Also utilized in the preparation of prodrugs due to its favorable polarity and hydrogen bonding capacity.

Used as a key intermediate in the synthesis of antiviral and antidiabetic drugs, particularly in the development of β-lactamase inhibitors and glucokinase activators. Its strained oxetane ring enhances metabolic stability and improves pharmacokinetic properties in drug candidates. Commonly employed in medicinal chemistry to increase solubility and binding affinity in small molecule therapeutics. Also utilized in the preparation of prodrugs due to its favorable polarity and hydrogen bonding capacity.

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...