(S)-2-Methoxy-3-(4-nitrophenyl)propanoic acid

97%

Reagent Code: #233367
fingerprint
CAS Number 2829279-64-1

science Other reagents with same CAS 2829279-64-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.2 g/mol
Formula C₁₀H₁₁NO₅
badge Registry Numbers
MDL Number MFCD32856421
thermostat Physical Properties
Boiling Point 410.8±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.336±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-blockers and other cardiovascular drugs. Its enantiomeric purity is critical for achieving desired biological activity in active pharmaceutical ingredients. Commonly employed in asymmetric synthesis routes where the (S)-configuration ensures optimal binding to target receptors. Also utilized in the preparation of enzyme inhibitors and in medicinal chemistry research for structure-activity relationship studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿23,370.00
(S)-2-Methoxy-3-(4-nitrophenyl)propanoic acid
No image available

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-blockers and other cardiovascular drugs. Its enantiomeric purity is critical for achieving desired biological activity in active pharmaceutical ingredients. Commonly employed in asymmetric synthesis routes where the (S)-configuration ensures optimal binding to target receptors. Also utilized in the preparation of enzyme inhibitors and in medicinal chemistry research for structure-activity r

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-blockers and other cardiovascular drugs. Its enantiomeric purity is critical for achieving desired biological activity in active pharmaceutical ingredients. Commonly employed in asymmetric synthesis routes where the (S)-configuration ensures optimal binding to target receptors. Also utilized in the preparation of enzyme inhibitors and in medicinal chemistry research for structure-activity relationship studies.

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...