(S)-2-(((4-methoxybenzyl)oxy)methyl)oxirane

95%

Reagent Code: #236257
fingerprint
CAS Number 144069-33-0

science Other reagents with same CAS 144069-33-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.23 g/mol
Formula C₁₁H₁₄O₃
badge Registry Numbers
MDL Number MFCD34182934
thermostat Physical Properties
Boiling Point 299.2±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.123±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used in the synthesis of complex organic molecules, particularly in pharmaceuticals where chiral intermediates are required. Its epoxide ring allows for regioselective and stereoselective ring-opening reactions, enabling the construction of specific stereocenters in target compounds. The 4-methoxybenzyl (PMB) protected hydroxymethyl group acts as a masked primary alcohol, preventing unwanted reactions during synthesis and allowing deprotection at a later stage for further functionalization. Commonly employed in the development of bioactive molecules, such as antivirals, and natural product syntheses due to its structural versatility.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,480.00
inventory 5g
10-20 days ฿4,450.00
inventory 25g
10-20 days ฿8,000.00
(S)-2-(((4-methoxybenzyl)oxy)methyl)oxirane
No image available
Used in the synthesis of complex organic molecules, particularly in pharmaceuticals where chiral intermediates are required. Its epoxide ring allows for regioselective and stereoselective ring-opening reactions, enabling the construction of specific stereocenters in target compounds. The 4-methoxybenzyl (PMB) protected hydroxymethyl group acts as a masked primary alcohol, preventing unwanted reactions during synthesis and allowing deprotection at a later stage for further functionalization. Commonly employe
Used in the synthesis of complex organic molecules, particularly in pharmaceuticals where chiral intermediates are required. Its epoxide ring allows for regioselective and stereoselective ring-opening reactions, enabling the construction of specific stereocenters in target compounds. The 4-methoxybenzyl (PMB) protected hydroxymethyl group acts as a masked primary alcohol, preventing unwanted reactions during synthesis and allowing deprotection at a later stage for further functionalization. Commonly employed in the development of bioactive molecules, such as antivirals, and natural product syntheses due to its structural versatility.
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...