Introduction of CAS:121579-86-0 | tert-Butyl 4-(chloromethyl)benzoate
Tert-butyl 4-(chloromethyl)benzoate is utilized in various synthesis processes. A method involving tert-butyl benzoates, like tert-butyl 4-(chloromethyl)benzoate, is employed for converting these compounds into derivatives with alkyl or substituted alkyl groups. This method has been applied in the synthesis of antimicrobial agents such as the fungal metabolite culpin.
In the field of photovoltaics, tert-butyl 4-C(61)-benzoate organofullerenes, including monoadduct, diadduct, and triadduct compounds, have been synthesized and examined for their photophysical, electrochemical, and thermal properties. These compounds are instrumental in the fabrication of photovoltaic devices, showing potential in energy conversion efficiencies.
Specification of CAS:121579-86-0 | tert-Butyl 4-(chloromethyl)benzoate
|
ITEMS |
SPECIFICATION |
|
Flash point |
320℃ |
|
Boiling point |
310℃ |
|
Density |
320℃ |
|
Storage condition |
under inert gas (nitrogen or Argon) at 2-8°C |
Research Application of CAS:121579-86-0 | tert-Butyl 4-(chloromethyl)benzoate
Chemical Stability Studies
The stability of certain compounds in scientific research is a critical factor. In this regard, potassium 5-tert-butyl-2-(tert-butyl-aminoxy)-benzoate, derived from tert-butyl 4-(chloromethyl)benzoate, was found to be significantly stable in water, which is crucial for various experimental setups (Marx & Rassat, 2002).
Material Science
In the field of material science, tert-butyl benzoates are used in the synthesis of novel polymers and materials. For example, 4-tert-butyl-1,2-bis(4-carboxyphenoxy)benzene and related compounds, which can be synthesized using tert-butyl benzoate derivatives, are key in producing polyamides with unique properties like high thermal stability and solubility in various solvents (Hsiao et al., 2000).
Electrochemical Studies
Tert-butyl benzoate derivatives are also valuable in electrochemical studies. The voltammetric reduction of phenyl-substituted 4-benzoyloxy-1-methylcyclohexyl bromides, which involves tert-butyl benzoate, aids in understanding the mechanisms of electron transfer and bond cleavage in chemical reactions (Antonello & Maran, 1998).
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