Potassium (S)-oxirane-2-carboxylate

97%

Reagent Code: #227640
fingerprint
CAS Number 82079-45-6

science Other reagents with same CAS 82079-45-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 126.16 g/mol
Formula C₃H₃KO₃
badge Registry Numbers
MDL Number MFCD00274195
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers and other bioactive molecules. Its epoxide ring allows for regioselective and stereoselective ring-opening reactions, enabling the introduction of functional groups with high enantiomeric purity. Commonly employed in asymmetric synthesis to construct complex organic molecules where stereochemistry is critical for biological activity. Also utilized in the development of enzyme inhibitors and as an intermediate in the preparation of natural product analogs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,770.00
inventory 1g
10-20 days ฿6,990.00
inventory 5g
10-20 days ฿30,340.00
Potassium (S)-oxirane-2-carboxylate
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers and other bioactive molecules. Its epoxide ring allows for regioselective and stereoselective ring-opening reactions, enabling the introduction of functional groups with high enantiomeric purity. Commonly employed in asymmetric synthesis to construct complex organic molecules where stereochemistry is critical for biological activity. Also utilized in the development of enzyme inhibitors and a

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers and other bioactive molecules. Its epoxide ring allows for regioselective and stereoselective ring-opening reactions, enabling the introduction of functional groups with high enantiomeric purity. Commonly employed in asymmetric synthesis to construct complex organic molecules where stereochemistry is critical for biological activity. Also utilized in the development of enzyme inhibitors and as an intermediate in the preparation of natural product analogs.

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...