(R)-3-(6-(2-((2,6-dichlorobenzyl)oxy)ethoxy)hexyl)-5-(2,2-dimethyl-4H-benzo[d][1,3]dioxin-6-yl)oxazolidin-2-one

≥95%

Reagent Code: #230559
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CAS Number 503068-36-8

science Other reagents with same CAS 503068-36-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 552.49 g/mol
Formula C₂₈H₃₅Cl₂NO₆
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in the synthesis of pharmaceutical intermediates for cardiovascular drugs, particularly as a chiral building block in the development of beta-blockers. Its structural features enable high selectivity in receptor binding, improving drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis due to the stable oxazolidinone ring, which acts as a directing group in stereoselective reactions. Also utilized in research settings for developing novel analogs with improved metabolic stability and bioavailability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿79,370.00
(R)-3-(6-(2-((2,6-dichlorobenzyl)oxy)ethoxy)hexyl)-5-(2,2-dimethyl-4H-benzo[d][1,3]dioxin-6-yl)oxazolidin-2-one
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Used in the synthesis of pharmaceutical intermediates for cardiovascular drugs, particularly as a chiral building block in the development of beta-blockers. Its structural features enable high selectivity in receptor binding, improving drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis due to the stable oxazolidinone ring, which acts as a directing group in stereoselective reactions. Also utilized in research settings for developing novel analogs with improved metabolic st

Used in the synthesis of pharmaceutical intermediates for cardiovascular drugs, particularly as a chiral building block in the development of beta-blockers. Its structural features enable high selectivity in receptor binding, improving drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis due to the stable oxazolidinone ring, which acts as a directing group in stereoselective reactions. Also utilized in research settings for developing novel analogs with improved metabolic stability and bioavailability.

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