(R)-3-Hydroxy-2-phenylpropanoic acid

95%

Reagent Code: #230824
fingerprint
CAS Number 17126-67-9

science Other reagents with same CAS 17126-67-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.17 g/mol
Formula C₉H₁₀O₃
badge Registry Numbers
MDL Number MFCD00211261
thermostat Physical Properties
Melting Point >120 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers and other cardiovascular drugs. Its stereochemistry allows for selective interactions in biological systems, making it valuable in asymmetric synthesis. Also employed in the preparation of enzyme inhibitors and as an intermediate in the development of anti-inflammatory agents. Commonly utilized in research for developing new optically active compounds due to its stable chiral center and functional group versatility.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,260.00
250mg
10-20 days ฿6,690.00
1g
10-20 days ฿19,990.00
(R)-3-Hydroxy-2-phenylpropanoic acid
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers and other cardiovascular drugs. Its stereochemistry allows for selective interactions in biological systems, making it valuable in asymmetric synthesis. Also employed in the preparation of enzyme inhibitors and as an intermediate in the development of anti-inflammatory agents. Commonly utilized in research for developing new optically active compounds due to its stable chiral center and funct

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers and other cardiovascular drugs. Its stereochemistry allows for selective interactions in biological systems, making it valuable in asymmetric synthesis. Also employed in the preparation of enzyme inhibitors and as an intermediate in the development of anti-inflammatory agents. Commonly utilized in research for developing new optically active compounds due to its stable chiral center and functional group 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...