Oxalyl chloride solution

2.0 M in methylene chloride, MkSeal

Reagent Code: #221109
label
Alias Oxalyl chloride; oxalyl chloride, diacyl dichloride
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CAS Number 79-37-8

science Other reagents with same CAS 79-37-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 126.93 g/mol
Formula C₂O₂Cl₂
badge Registry Numbers
EC Number 201-200-2
MDL Number MFCD00000704
thermostat Physical Properties
Boiling Point 39.8-40 °C
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Widely used in organic synthesis, this reagent efficiently converts carboxylic acids to acid chlorides, making it valuable in the preparation of amides, esters, and peptides. It is also employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals due to its high reactivity and selectivity. Commonly used in Vilsmeier-Haack type reactions, it helps introduce formyl groups in aromatic systems. Its liquid state and solubility in common organic solvents make it convenient for use in solution-phase reactions. Due to its moisture sensitivity, it is typically handled under anhydrous conditions in inert atmospheres.

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Size Availability Unit Price Quantity
inventory 100ml
10-20 days ฿1,450.00
inventory 500ml
10-20 days ฿3,980.00

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Oxalyl chloride solution
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Widely used in organic synthesis, this reagent efficiently converts carboxylic acids to acid chlorides, making it valuable in the preparation of amides, esters, and peptides. It is also employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals due to its high reactivity and selectivity. Commonly used in Vilsmeier-Haack type reactions, it helps introduce formyl groups in aromatic systems. Its liquid state and solubility in common organic solvents make it convenient for use in solutio

Widely used in organic synthesis, this reagent efficiently converts carboxylic acids to acid chlorides, making it valuable in the preparation of amides, esters, and peptides. It is also employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals due to its high reactivity and selectivity. Commonly used in Vilsmeier-Haack type reactions, it helps introduce formyl groups in aromatic systems. Its liquid state and solubility in common organic solvents make it convenient for use in solution-phase reactions. Due to its moisture sensitivity, it is typically handled under anhydrous conditions in inert atmospheres.

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