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Bis(2-methoxyphenyl) carbonate

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Identification
Molecular formula
C15H14O5
CAS number
2167-68-2
IUPAC name
bis(2-methoxyphenyl) carbonate
State
State

At room temperature, bis(2-methoxyphenyl) carbonate is typically found in a solid state.

Melting point (Celsius)
68.00
Melting point (Kelvin)
341.15
Boiling point (Celsius)
375.00
Boiling point (Kelvin)
648.15
General information
Molecular weight
258.27g/mol
Molar mass
258.2540g/mol
Density
1.2100g/cm3
Appearence

Bis(2-methoxyphenyl) carbonate typically appears as a white crystalline solid, characterized by its lustrous surface.

Comment on solubility

Solubility of Bis(2-methoxyphenyl) Carbonate

Bis(2-methoxyphenyl) carbonate, with its intriguing structure, exhibits unique solubility characteristics that can be crucial for various applications. Its solubility is influenced by several factors:

  • Solvent Interaction: This compound tends to be more soluble in organic solvents like ethanol, methanol, and acetone, rather than in polar solvents such as water.
  • Temperature Dependency: The solubility may increase with an increase in temperature, which is a common trait for many organic compounds.
  • Hydrophobic Nature: Due to its aromatic rings, bis(2-methoxyphenyl) carbonate displays a certain degree of hydrophobicity, which typically leads to limited solubility in aqueous environments.

In summary, as a carbonic ester, bis(2-methoxyphenyl) carbonate illustrates significant solubility in non-polar to moderately polar solvents, while being relatively insoluble in water. This solubility pattern is essential for its applications in fields such as materials science and organic synthesis.

Interesting facts

Interesting Facts about Bis(2-methoxyphenyl) Carbonate

Bis(2-methoxyphenyl) carbonate is a fascinating organic compound that belongs to the category of carbonates. Here are some captivating facts about this compound:

  • Applications in Material Science: This compound is notably used as a precursor in the synthesis of various polymers, particularly in producing polycarbonate materials. Polycarbonates are famous for their strength and transparency, making them ideal for applications such as eyewear lenses and safety equipment.
  • Chemical Structure: The structure of bis(2-methoxyphenyl) carbonate consists of two methoxyphenyl groups connected by a carbonate functional group. This unique structure contributes to its stability and reactivity in chemical processes.
  • Reactivity and Synthesis: It can be synthesized through the reaction of phenol derivatives with phosgene or similar carbonylating agents, showcasing the versatility of aromatic compounds in organic synthesis.
  • Environmental Considerations: Awareness surrounding green chemistry has led to interest in eco-friendly pathways for synthesizing compounds like bis(2-methoxyphenyl) carbonate, aiming to reduce harmful byproducts.
  • Research and Development: Ongoing research is exploring its potential in drug delivery systems and as a building block for advanced materials, indicating its relevance beyond conventional applications.
  • Historical Context: Bis(2-methoxyphenyl) carbonate has gained attention over the years since its introduction into the realm of organic compounds, leading to various studies focusing on its properties and potential applications in different sectors.

In summary, bis(2-methoxyphenyl) carbonate is not only a compound of significant industrial importance but also a subject of ongoing scientific inquiry. Its role in the development of new materials and its potential for various applications make it an exciting compound for chemists and materials scientists alike.

Synonyms
GUAIACOL CARBONATE
Bis(2-methoxyphenyl) carbonate
Duotal
Tussophob
Guaiacyl carbonate
Bis-o-methoxyphenyl carbonate
Di-o-methoxyphenyl carbonate
Diguaiacyl carbonate
Guaiacol carbonic acid neutral ester
Phenol, 2-methoxy-, carbonate (2:1)
Carbonic acid bis(2-methoxyphenyl) ester
Guaiacol carbonate [NF]
Carbonic acid, bis(o-methoxyphenyl) ester
UNII-Q71XPQ6R29
NSC 37138
Q71XPQ6R29
DTXSID3046405
NSC-3798
EINECS 209-034-2
NSC-37138
Carbonic acid guiacol ether
GUAIACOL CARBONATE [MI]
DTXCID1026405
GUAIACOL CARBONATE [WHO-DD]
NSC37138
Carbonic acid bis(2-methyoxyphenyl) ester
Carbonic acid bis[2-methoxyphenyl] ester
Phenol, 2-methoxy-, carbonate (2:1) (9CI)
Carbonic acid, bis(o-methoxyphenyl) ester (8CI)
orujfmpwkpvxlz-uhfffaoysa-n
553-17-3
MLS002637719
NCGC00164512-01
NCGC00164512-02
guaiacolcarbonate
Phenol, carbonate (2:1)
CAS-553-17-3
Guajacolcarbonat
SCHEMBL21541
CHEMBL1898058
NSC3798
CHEBI:135131
HMS3078E13
CS-B1684
HY-Y1876
Tox21_112147
MFCD00025723
AKOS005068004
Tox21_112147_1
Bis(o-methoxyphenyl)ester carbonic acid
CS-16937
SMR001547241
DB-052713
NS00033290
C13264
SBI-0654036.0001
Q27287071