25574-16-7

Usage

Molecular Weight

213.1 g/mol The molecular weight of 2-(4-bromophenyl)oxetane is 213.1 grams per mole, which is the sum of the atomic weights of all the atoms in the molecule.

Appearance

Colorless liquid 2-(4-bromophenyl)oxetane is a colorless liquid, which means that it does not have any color when it is in its pure form.

Boiling Point

64-66°C at 10 mmHg The boiling point of 2-(4-bromophenyl)oxetane is the temperature at which it changes from a liquid to a gas at a pressure of 10 millimeters of mercury. In this case, the boiling point is between 64 and 66 degrees Celsius.

Density

1.35 g/cm3 The density of 2-(4-bromophenyl)oxetane is the mass per unit volume of the compound, which is 1.35 grams per cubic centimeter.

Solubility

Insoluble in water, soluble in organic solvents 2-(4-bromophenyl)oxetane is insoluble in water, which means that it does not dissolve in water, but it is soluble in organic solvents, such as ethanol, diethyl ether, and acetone.

Reactivity

Can undergo various chemical reactions 2-(4-bromophenyl)oxetane is a reactive compound that can participate in various chemical reactions, such as electrophilic substitution, nucleophilic substitution, and elimination reactions. This makes it a valuable building block for the synthesis of diverse organic molecules.

Uses

Organic synthesis, pharmaceuticals, agrochemicals, and fine chemicals 2-(4-bromophenyl)oxetane is commonly used in organic synthesis and can be utilized as a reagent in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it a valuable building block for the synthesis of diverse organic molecules with potential applications in various industries.

Biological Activities

Studied for potential biological activities and pharmacological properties 2-(4-bromophenyl)oxetane has been studied for its potential biological activities and pharmacological properties, which means that it may have potential as a therapeutic agent or as a chemical probe for studying biological processes.

Upstream product

• 25574-19-0 1-(4-bromophenyl)-3-chloro-1-propanol 
• 31736-73-9 4-bromophenyl 2-chloroethyl ketone 

Downstream Products

• 105515-33-1 (2E)-3-(4-bromophenyl)prop-2-en-1-ol 
• 4489-22-9 (+/-)-1-(4-bromophenyl)propanol 

Relevant academic research and scientific papers

AZAINDOLE DERIVATIVE HAVING AMPK-ACTIVATING EFFECT

Disclosed is a compound which is useful as an AMPK activator. A compound represented by formula: or its pharmaceutically acceptable salt, wherein X is substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, or substituted or unsubstituted heterocyclyl; R1 is hydrogen, halogen, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted acyl, substituted or unsubstituted carbamoyl, substituted or unsubstituted alkylthio, substituted or unsubstituted alkylsulfinyl, substituted or unsubstituted alkylsulfonyl, or substituted or unsubstituted alkyloxycarbonyl; R2 is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted heterocyclyl, or the like; R3 is halogen, hydroxy, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted heterocyclyl, or the like; and R4 is hydrogen, halogen, hydroxy, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, or the like.