Benzenepropanoic acid,a-hydroxy-b-methoxy-b-phenyl-,(aS)-

98%

Reagent Code: #143740
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CAS Number 178306-52-0

science Other reagents with same CAS 178306-52-0

blur_circular Chemical Specifications

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Weight 272.298 g/mol
Formula C₁₆H₁₆O₄
inventory_2 Storage & Handling
Density 1.248
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the production of certain cardiovascular and anti-inflammatory drugs. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy. Commonly employed in the development of beta-blockers and other bioactive molecules requiring specific enantiomeric forms. Also utilized in research settings for the preparation of chiral ligands and catalysts in organic reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿154.00
inventory 5g
10-20 days ฿950.00
inventory 25g
10-20 days ฿4,720.00

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Benzenepropanoic acid,a-hydroxy-b-methoxy-b-phenyl-,(aS)-
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Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the production of certain cardiovascular and anti-inflammatory drugs. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy. Commonly employed in the development of beta-blockers and other bioactive molecules requiring specific enantiomeric forms. Also utilized in research settings for the preparation of chiral ligands and catalysts in organic reactio

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the production of certain cardiovascular and anti-inflammatory drugs. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy. Commonly employed in the development of beta-blockers and other bioactive molecules requiring specific enantiomeric forms. Also utilized in research settings for the preparation of chiral ligands and catalysts in organic reactions.

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