1-(((4-Chlorophenoxy)carbonyl)oxy)ethyl isobutyrate

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Reagent Code: #161899
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CAS Number 1622940-14-0

science Other reagents with same CAS 1622940-14-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.71 g/mol
Formula C₁₃H₁₅ClO₅
badge Registry Numbers
MDL Number MFCD29920546
thermostat Physical Properties
Boiling Point 364.5±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a reactive ester in organic transformations. Its structure allows for efficient introduction of phenoxy-based moieties into larger molecules, making it valuable in the development of herbicides and plant growth regulators. The chlorophenoxy group enhances lipophilicity, aiding in membrane penetration in bioactive compounds. It is also employed in controlled release formulations due to its ability to undergo enzymatic or hydrolytic cleavage, enabling timed delivery of active agents. Its application extends to polymer chemistry as a crosslinking or modifying agent in specialty resins.

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inventory 5g
10-20 days ฿42,000.00

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1-(((4-Chlorophenoxy)carbonyl)oxy)ethyl isobutyrate
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Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a reactive ester in organic transformations. Its structure allows for efficient introduction of phenoxy-based moieties into larger molecules, making it valuable in the development of herbicides and plant growth regulators. The chlorophenoxy group enhances lipophilicity, aiding in membrane penetration in bioactive compounds. It is also employed in controlled release formulations due to its abil

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a reactive ester in organic transformations. Its structure allows for efficient introduction of phenoxy-based moieties into larger molecules, making it valuable in the development of herbicides and plant growth regulators. The chlorophenoxy group enhances lipophilicity, aiding in membrane penetration in bioactive compounds. It is also employed in controlled release formulations due to its ability to undergo enzymatic or hydrolytic cleavage, enabling timed delivery of active agents. Its application extends to polymer chemistry as a crosslinking or modifying agent in specialty resins.

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