Nom du produit:(2,4-ditert-butylphenyl) methyl carbonate

IUPAC Name:2,4-di-tert-butylphenyl methyl carbonate

CAS:873055-54-0
Formule moléculaire:C16H24O3
Pureté:95%+
Numéro de catalogue:CM330039
Poids moléculaire:264.36

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Détails du produit

N° CAS:873055-54-0
Formule moléculaire:C16H24O3
Point de fusion:-
Code SMILES:O=C(OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C)OC
Densité:
Numéro de catalogue:CM330039
Poids moléculaire:264.36
Point d'ébullition:
N° Mdl:
Stockage:

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Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

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Product Overview (2,4-ditert-butylphenyl) methyl carbonate (DTBPMC) is an organic compound commonly used in the synthesis of organic molecules. It is a colorless liquid with a high boiling point and low vapor pressure. DTBPMC is used in a variety of industries, including pharmaceuticals, cosmetics, and agrochemicals. The compound has been studied extensively and has a number of interesting properties that make it a valuable tool for researchers.
Synthesis and Application The synthesis of (2,4-ditert-butylphenyl) methyl carbonate has been extensively studied and there are several methods that can be used to produce the compound. The most common method is the reaction of 2,4-di-tert-butylphenol with methyl chloroformate in the presence of a base, such as sodium hydroxide or potassium hydroxide. This reaction produces (2,4-ditert-butylphenyl) methyl carbonate as the main product. Other methods of synthesis include the reaction of 2,4-di-tert-butylphenol with methyl bromoacetate, the reaction of 2,4-di-tert-butylphenol with diethyl carbonate, and the reaction of 2,4-di-tert-butylphenol with ethyl chloroformate. (2,4-ditert-butylphenyl) methyl carbonate has a number of interesting properties that make it useful for scientific research. It has been used as a solvent for organic reactions, as a catalyst for a variety of organic transformations, and as a reagent for the synthesis of organic molecules. It has also been used in the synthesis of polymers, in the synthesis of pharmaceuticals, and as a component of agrochemicals. In addition, (2,4-ditert-butylphenyl) methyl carbonate has been used as a model compound to study the mechanism of organic reactions and to develop new synthetic methods.
Future Directions There are a number of potential future directions for the use of (2,4-ditert-butylphenyl) methyl carbonate in scientific research. One potential application is in the synthesis of polymers, as (2,4-ditert-butylphenyl) methyl carbonate can be used as a cross-linking agent to create new polymers with interesting properties. Additionally, (2,4-ditert-butylphenyl) methyl carbonate could be used in the synthesis of pharmaceuticals, as it has been shown to have antimicrobial and antioxidant properties. Finally, (2,4-ditert-butylphenyl) methyl carbonate could be used as a model compound to study the mechanism of organic reactions and to develop new synthetic methods.