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1-Bicyclo[2.2.2]octylammonium chloride is a quaternary ammonium compound with the chemical formula C8H16ClN. It is derived from the bicyclic structure of bicyclo[2.2.2]octane, where one of the hydrogen atoms on the nitrogen atom is replaced by a chloride ion, resulting in a positively charged ammonium group. 1-bicyclo<2.2.2>octylammonium chloride is known for its surfactant properties and is used in various applications, including as a phase-transfer catalyst, a reagent in organic synthesis, and in the preparation of certain types of ionic liquids. Due to its unique structure and cationic nature, 1-bicyclo[2.2.2]octylammonium chloride can interact with a range of anions and molecules, making it a versatile component in chemical processes and formulations.

1193-43-7

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1193-43-7 Usage

Chemical structure

1-bicyclo<2.2.2>octylammonium chloride consists of a bicyclo<2.2.2>octane ring structure with an attached ammonium chloride group.

Solubility

Highly soluble in organic solvents.

Application

Commonly used as a phase transfer catalyst in organic chemistry reactions.

Function

Facilitates the transfer of reactants between two immiscible phases.

Synthetic processes

Utilized in various synthetic processes such as oxidation, alkylation, and halogenation reactions.

Potential application

Investigated for its potential application in the synthesis of nanomaterials.

Material properties modification

Used as a modifier for the properties of certain materials.

Role

Plays a crucial role in facilitating and optimizing organic synthesis and material science research.

Check Digit Verification of cas no

The CAS Registry Mumber 1193-43-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1193-43:
(6*1)+(5*1)+(4*9)+(3*3)+(2*4)+(1*3)=67
67 % 10 = 7
So 1193-43-7 is a valid CAS Registry Number.

1193-43-7Relevant academic research and scientific papers

cis-Diazenes. Pressure Effects on Their Thermal Deazatization and Isomerization Reactions

Neuman, Robert C.,Berge, Charles T.,Binegar, Glen Al.,Adam, Waldemar,Nishizawa, Yoshinori

, p. 4564 - 4568 (1990)

Effects of pressure on solution-phase rates of overall thermal decomposition, deazatization, and isomerization of several symmetric cis-diazenes (cis-azoalkanes) have been determined in hexane and in ethanol.Increasing pressure decreases all the rates.The large positive activation volumes for deazatization (e.g., +16 to +22 cm3/mol) have been interpreted in terms of a one-bond scission mechanism and an intermediate diazenyl radical.The smaller positive activation volumes for isomerization (e.g., +5 to +7 cm3/mol) are consistent with a nonradical inversion mechanism.Dramatic differences in rates between polar and nonpolar solvents are consistent with these mechanisms.

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