(R)-3-(4-(Benzyloxy)phenyl)-2-hydroxypropanoic acid

95%

Reagent Code: #229805
fingerprint
CAS Number 373368-68-4

science Other reagents with same CAS 373368-68-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.30 g/mol
Formula C₁₆H₁₆O₄
badge Registry Numbers
MDL Number MFCD14636472
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-blockers and other cardiovascular drugs. Its stereochemistry allows for selective biological activity, making it valuable in producing enantiomerically pure compounds. The hydroxy and carboxylic acid functional groups enable further chemical modifications, facilitating its incorporation into more complex drug molecules. Commonly employed in research and industrial settings for asymmetric synthesis and optimization of active pharmaceutical ingredients.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿12,620.00
1g
10-20 days ฿54,450.00
(R)-3-(4-(Benzyloxy)phenyl)-2-hydroxypropanoic acid
No image available

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-blockers and other cardiovascular drugs. Its stereochemistry allows for selective biological activity, making it valuable in producing enantiomerically pure compounds. The hydroxy and carboxylic acid functional groups enable further chemical modifications, facilitating its incorporation into more complex drug molecules. Commonly employed in research and industrial settings for asymmetric synthesis a

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-blockers and other cardiovascular drugs. Its stereochemistry allows for selective biological activity, making it valuable in producing enantiomerically pure compounds. The hydroxy and carboxylic acid functional groups enable further chemical modifications, facilitating its incorporation into more complex drug molecules. Commonly employed in research and industrial settings for asymmetric synthesis and optimization of active pharmaceutical ingredients.

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...