Skip to main content

Methyl 4-(4-methoxycarbonylphenyl)benzoate

ADVERTISEMENT
Identification
Molecular formula
C16H14O4
CAS number
607-97-6
IUPAC name
methyl 4-(4-methoxycarbonylphenyl)benzoate
State
State

At room temperature, it is in a solid state. This compound typically forms white crystalline structures.

Melting point (Celsius)
193.00
Melting point (Kelvin)
466.15
Boiling point (Celsius)
374.50
Boiling point (Kelvin)
647.65
General information
Molecular weight
286.29g/mol
Molar mass
286.2920g/mol
Density
1.2760g/cm3
Appearence

This compound appears as a white crystalline powder or solid at room temperature. It is often used in organic synthesis and may present in a fine granular form.

Comment on solubility

Solubility of Methyl 4-(4-methoxycarbonylphenyl)benzoate

Methyl 4-(4-methoxycarbonylphenyl)benzoate, with its complex and aromatic structure, exhibits unique solubility characteristics that make it interesting for various applications. Solubility is a fundamental property that reflects how a substance interacts with solvents, which is crucial for processes like extraction, crystallization, and formulation.

Here are some key points regarding the solubility of this compound:

  • Solvent Compatibility: Methyl 4-(4-methoxycarbonylphenyl)benzoate is typically soluble in organic solvents such as ethanol, acetone, and chloroform. Its solubility in these solvents makes it suitable for various synthetic and industrial processes.
  • Water Solubility: This compound has very limited solubility in water. The presence of lipophilic groups in its structure contributes to its poor interaction with polar solvent molecules.
  • Temperature Dependence: Like many organic compounds, solubility can be influenced by temperature. An increase in temperature may enhance solubility in organic solvents, leading to better dissolution properties.

As a result, understanding the solubility of methyl 4-(4-methoxycarbonylphenyl)benzoate is important for applications in fields like organic chemistry and materials science. The compound stands as a representative example of how functional groups and molecular structure significantly affect solubility behavior.

Interesting facts

Interesting Facts About Methyl 4-(4-methoxycarbonylphenyl)benzoate

Methyl 4-(4-methoxycarbonylphenyl)benzoate is a fascinating compound in the realm of organic chemistry, primarily due to its various applications and unique properties. Here are some intriguing aspects of this compound:

  • Structural Significance: This compound possesses a complex structure that includes both ester and aromatic functionalities. Its structure allows it to engage in various chemical reactions, making it a valuable precursor for synthesizing other compounds.
  • Role in Synthesis: Methyl 4-(4-methoxycarbonylphenyl)benzoate serves as an intermediate in the production of pharmaceuticals and agrochemicals. Its reactivity often leads to the creation of biologically active molecules, showcasing its importance in medicinal chemistry.
  • Applications in Research: Researchers explore this compound for its electrochemical properties, contributing to advancements in materials science, particularly in the development of organic semiconductors and photovoltaics.
  • Natural Occurrence: Although primarily synthetic, some closely related compounds might be found in nature, hinting at an intriguing relationship between natural products and synthetic derivatives.
  • Potential Biological Activity: Studies have indicated that methyl esters like this one may exhibit pharmacological effects, leading to ongoing research in their potential as therapeutic agents.

In the words of a renowned chemist, "Every molecule tells a story; understanding its tale is key to unlocking new realms of knowledge." Methyl 4-(4-methoxycarbonylphenyl)benzoate exemplifies this sentiment, offering a rich narrative woven through chemical innovation and discovery. As research continues in this area, we can expect to glean more insights into both its properties and applications!

Synonyms
792-74-5
dimethyl [1,1'-biphenyl]-4,4'-dicarboxylate
Biphenyl dimethyl dicarboxylate
DIMETHYL 4,4'-BIPHENYLDICARBOXYLATE
Nissel
4,4'-Biphenyldicarboxylic acid, dimethyl ester
4,4'-Bis(methoxycarbonyl)biphenyl
K61BXA0U9C
HSDB 5754
Dimethyl (1,1'-biphenyl)-4,4'-dicarboxylate
EINECS 212-341-4
4,4'-dimethyl [1,1'-biphenyl]-4,4'-dicarboxylate
(1,1'-Biphenyl)-4,4'-dicarboxylic acid, 4,4'-dimethyl ester
DIMETHYL 4,4'-BIPHENYLDICARBOXYLATE [WHO-DD]
4,4'-Dimethyl (1,1'-biphenyl)-4,4'-dicarboxylate
[1,1'-Biphenyl]-4,4'-dicarboxylic acid, 4,4'-dimethyl ester
4,4'Biphenyldicarboxylic acid, dimethyl ester
(1,1'Biphenyl)4,4'dicarboxylic acid, dimethyl ester
Dimethyl biphenyl-4,4'-dicarboxylate
methyl 4-(4-methoxycarbonylphenyl)benzoate
[1,1'-Biphenyl]-4,4'-dicarboxylic acid, dimethyl ester
MFCD00017201
(1,1'-Biphenyl)-4,4'-dicarboxylic acid, dimethyl ester
UNII-K61BXA0U9C
4,4'-Bibenzoic Acid Dimethyl Ester
Dimethyl biphenyl-4,4''-dicarboxylate
Maybridge1_001712
4,4-Dicarboxymethylbiphenyl
4,4'-Dicarbomethoxybiphenyl
SCHEMBL68521
MLS000720058
CHEMBL4297409
DTXSID2061143
HMS546F18
4,4'-bis (methoxycarbonyl)biphenyl
CCG-45472
AKOS001588888
DB12475
FD62602
SMR000304587
SY057043
TS-00900
HY-128854
B1309
CS-0100928
Dimethyl biphenyl-4,4'-dicarboxylate, 99%
NS00038033
dimethyl[1,1'-biphenyl]-4,4'-dicarboxylate
4,4'-Biphenyldicarboxylic Acid Dimethyl Ester
F15436
Biphenyl 4,4'-dicarboxylic acid, dimethyl ester
SR-01000397421
SR-01000397421-1
SR-01000397421-2
BRD-K33126632-001-02-1
Q27281994
Dimethyl 4,4 inverted exclamation mark -Biphenyldicarboxylate
4,4'-Bibenzoic acid dimethyl ester;4,4'-Biphenyldicarboxylic acid dimethyl ester
Dimethyl 4,4'-biphenyldicarboxylate; Dimethyl [1,1'-biphenyl]-4,4'-dicarboxylate; Dimethyl 1,1'-Biphenyl]-4,4'-dicarboxylic Acid Ester; Dimethyl 4,4'-Biphenyldicarboxylic Acid Ester;