Oxiranecarboxylic acid, 2-[6-(4-chlorophenoxy)hexyl]-, ethyl ester, (2S)-

≥95%

Reagent Code: #221061
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CAS Number 828934-40-3

science Other reagents with same CAS 828934-40-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 326.8151 g/mol
Formula C₁₇H₂₃ClO₄
thermostat Physical Properties
Boiling Point 405.0±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.163±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-blockers and other cardiovascular drugs. Its chiral structure makes it valuable in enantioselective synthesis, where the (2S) configuration is critical for biological activity. The compound’s ester and epoxide functionalities allow for further chemical modifications, enabling the construction of complex molecules. It is also employed in research settings for exploring new synthetic routes and optimizing drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿80,000.00
250mg
10-20 days ฿136,000.00
Oxiranecarboxylic acid, 2-[6-(4-chlorophenoxy)hexyl]-, ethyl ester, (2S)-
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-blockers and other cardiovascular drugs. Its chiral structure makes it valuable in enantioselective synthesis, where the (2S) configuration is critical for biological activity. The compound’s ester and epoxide functionalities allow for further chemical modifications, enabling the construction of complex molecules. It is also employed in research settings for exploring new synthetic routes and optimizing d

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-blockers and other cardiovascular drugs. Its chiral structure makes it valuable in enantioselective synthesis, where the (2S) configuration is critical for biological activity. The compound’s ester and epoxide functionalities allow for further chemical modifications, enabling the construction of complex molecules. It is also employed in research settings for exploring new synthetic routes and optimizing drug candidates.

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