22750-93-2

Basic information

• Product Name: Hyperchloric acid ethyl ester
• Synonyms: Hyperchloric acid ethyl ester
• CAS NO: 22750-93-2
• Molecular Formula: C₂H₅ClO₄
• Molecular Weight: 128.5117
• Mol File: 22750-93-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 165.3°C (rough estimate)
• Appearance: /
• Density: 1.5090 (rough estimate)
• Refractive Index: 1.4100 (estimate)
• CAS DataBase Reference: Hyperchloric acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Hyperchloric acid ethyl ester(22750-93-2)
• EPA Substance Registry System: Hyperchloric acid ethyl ester(22750-93-2)

Safety Data

• Safety Statements: −. See also PERCHLORATES." target="_blank">Possibly the most explosive chemical known. Very sensitive to impact, friction,
• Hazardous Substances Data: 22750-93-2(Hazardous Substances Data)

Usage

Safety Profile

Possibly the most explosive chemical known. Very sensitive to impact, friction, and heat. Upon decomposition it emits toxic fumes of Cl-. See also PERCHLORATES.

Upstream product

• 74-96-4 ethyl bromide 
• 64-17-5 ethanol 
• 74-84-0 ethane 
• 75-03-6 ethyl iodide 
• 6509-22-4 barium ethyl sulfate 

Relevant articles and documents

Direct vs. Indirect Mechanisms in Organic Electrochemistry. Estimates of Activation Energies for Hydrogen Atom Transfer Processes of Relevance in Indirect Mechanisms Using the Bond Energy-Bond Order (BEBO) and Equibonding Methods

Activation energies for a number of hydrogen abstraction reactions of interest in mechanistic organic electrochemistry have been calculated using the bond energy-bond-order (BEBO) and equibonding method.The main emphasis has been put on processes with bearing on the problem of deciding between direct and indirect mechanisms in anodic oxidation, viz. acyloxylation, hydroxylation, methoxylation, nitrooxylation, cyanation, carbomethoxylation and azidation.The results indicate that indirect mechanisms might play a more important role than presently assumed.