sodium 4-(4-chloro-o-tolyloxy)butyrate

≥95%

Reagent Code: #232871
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CAS Number 6062-26-6

science Other reagents with same CAS 6062-26-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.6619 g/mol
Formula C₁₁H₁₃ClNaO₃
badge Registry Numbers
MDL Number MFCD00137249
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It plays a role in constructing ester and ether derivatives through its carboxylate and ether functional groups. Commonly utilized in research settings for modifying drug molecules to improve solubility and bioavailability. Also employed in the preparation of prodrugs where controlled release of the active compound is required. Its chlorinated aromatic structure supports stability and specific binding in biological systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿48,000.00
inventory 250mg
10-20 days ฿80,000.00
sodium 4-(4-chloro-o-tolyloxy)butyrate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It plays a role in constructing ester and ether derivatives through its carboxylate and ether functional groups. Commonly utilized in research settings for modifying drug molecules to improve solubility and bioavailability. Also employed in the preparation of prodrugs where controlled release of the active compound is required. Its chlorinated aromatic structure supports

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. It plays a role in constructing ester and ether derivatives through its carboxylate and ether functional groups. Commonly utilized in research settings for modifying drug molecules to improve solubility and bioavailability. Also employed in the preparation of prodrugs where controlled release of the active compound is required. Its chlorinated aromatic structure supports stability and specific binding in biological systems.

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