potassium 2-chloro-3-(benzyloxy)propionate

98%

Reagent Code: #228211
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CAS Number 138666-92-9

science Other reagents with same CAS 138666-92-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.7359 g/mol
Formula C₁₀H₁₀ClKO₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of β-blockers and other pharmaceutical agents. The compound's chloro and benzyloxy functional groups allow for selective transformations, making it valuable in constructing chiral molecules. It is employed in the synthesis of cardioselective drugs where the propionate backbone serves as a key structural element. The benzyl protecting group can be removed under mild conditions, enabling further functionalization in multi-step reactions. Its potassium salt form enhances solubility in polar solvents, facilitating reaction handling in aqueous or mixed solvent systems.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿52,870.00
potassium 2-chloro-3-(benzyloxy)propionate
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Used as an intermediate in organic synthesis, particularly in the preparation of β-blockers and other pharmaceutical agents. The compound's chloro and benzyloxy functional groups allow for selective transformations, making it valuable in constructing chiral molecules. It is employed in the synthesis of cardioselective drugs where the propionate backbone serves as a key structural element. The benzyl protecting group can be removed under mild conditions, enabling further functionalization in multi-step re

Used as an intermediate in organic synthesis, particularly in the preparation of β-blockers and other pharmaceutical agents. The compound's chloro and benzyloxy functional groups allow for selective transformations, making it valuable in constructing chiral molecules. It is employed in the synthesis of cardioselective drugs where the propionate backbone serves as a key structural element. The benzyl protecting group can be removed under mild conditions, enabling further functionalization in multi-step reactions. Its potassium salt form enhances solubility in polar solvents, facilitating reaction handling in aqueous or mixed solvent systems.

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