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3,4-Dimethoxyphenylacetic acid

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Identification
Molecular formula
C10H12O4
CAS number
93-40-3
IUPAC name
2-(3,4-dimethoxyphenyl)acetic acid
State
State

At room temperature, 3,4-Dimethoxyphenylacetic acid is a solid. It is stable under normal conditions and has a crystalline structure, reflecting its aromatic and carboxylic functional groups. The presence of methoxy groups may influence its physical properties, giving it a distinct texture typical of crystalline solids.

Melting point (Celsius)
70.00
Melting point (Kelvin)
343.15
Boiling point (Celsius)
176.00
Boiling point (Kelvin)
449.15
General information
Molecular weight
196.21g/mol
Molar mass
196.2060g/mol
Density
1.2214g/cm3
Appearence

3,4-Dimethoxyphenylacetic acid is a crystalline powder at room temperature. It appears as a white to off-white crystalline solid. The compound's solid state is due to the aromatic ring and methoxy groups present in its structure, contributing to its crystallinity.

Comment on solubility

Solubility of 2-(3,4-Dimethoxyphenyl)acetic Acid

When it comes to the solubility of 2-(3,4-dimethoxyphenyl)acetic acid, several fascinating characteristics emerge. Generally speaking, this compound displays the following solubility traits:

  • Solvent Compatibility: It is primarily soluble in organic solvents, such as methanol, ethanol, and dichloromethane.
  • Limited Aqueous Solubility: Its solubility in water is relatively low, which is common for many organic acids with complex structures.
  • Temperature Dependence: As with many organic compounds, increased temperature typically enhances solubility; therefore, heating the solvent might aid in dissolving 2-(3,4-dimethoxyphenyl)acetic acid.

It is essential to recognize the implications of solubility in chemical reactions and formulations. A quote often summarized in chemistry is, “Like dissolves like,” which means that the structure and polarity of a solute affect its solubility in different solvents. Consequently, understanding the solubility of this compound can be vital in applications ranging from pharmaceuticals to organic synthesis.

In summary, while 2-(3,4-dimethoxyphenyl)acetic acid may prove challenging to dissolve in water, its solubility in organic solvents allows for versatile applications in various chemical processes.

Interesting facts

Interesting Facts about 2-(3,4-dimethoxyphenyl)acetic acid

2-(3,4-dimethoxyphenyl)acetic acid is a fascinating compound that has garnered attention in various fields of research. It belongs to the class of aromatic carboxylic acids and exhibits interesting chemical properties:

  • Biological Activity: This compound has been studied for its potential anti-inflammatory and analgesic effects. Research indicates that derivatives of this compound may play a role in pain management.
  • Synthetic Applications: It serves as a useful building block in organic synthesis, particularly in the synthesis of pharmaceuticals and other complex organic molecules.
  • Research Utility: Scientists are exploring its potential as a molecular scaffold for developing new drugs, making it a significant compound in medicinal chemistry studies.
  • Substituent Influence: The presence of methoxy groups at the 3 and 4 positions of the phenyl ring enhances the compound's solubility and modifies its reactivity, which can lead to different biological activities or therapeutic effects.

As you dive deeper into the world of organic chemistry, remember that compounds like 2-(3,4-dimethoxyphenyl)acetic acid not only serve as interesting subjects for study but also exemplify the intricate relationships between structure and biological activity. As one researcher put it, "Understanding these relationships can open doors to innovative therapeutic solutions."

Synonyms
93-40-3
Homoveratric acid
3,4-Dimethoxyphenylacetic acid
2-(3,4-dimethoxyphenyl)acetic acid
(3,4-DIMETHOXYPHENYL)ACETIC ACID
Benzeneacetic acid, 3,4-dimethoxy-
(3,4-Dimethoxyphenyl) Acetic Acid
3,4-Dimethoxybenzeneacetic acid
3,4-Dimethoxyphenylaceticacid
3,4-Dimethoxyphenyl acetic acid
Acetic acid, (3,4-dimethoxyphenyl)-
Homoveratrumic acid
(3,4-Dimethoxy-phenyl)-acetic acid
NSC 2753
EINECS 202-244-5
YY50GIT3C7
MFCD00004335
BRN 1110282
AI3-23354
3,4-(Dimethoxy)benzeneacetic acid
NSC-2753
NSC-27897
DTXSID5059086
CHEBI:86655
2-(3,4-DIMETHOXYPHENYL)ETHANOIC ACID
Benzeneacetic acid,4-dimethoxy-
Acetic acid,4-dimethoxyphenyl)-
3,4-(Dimethoxyphenyl) acetic acid
(3,?4-?Dimethoxyphenyl)?acetic Acid(Homoveratric Acid)
Homoveratrate
homovaretic acid
2-(3,4-Dimethoxyphenyl)acetate; 2-(3,4-Dimethoxyphenyl)acetic Acid; 3,4-Dimethoxybenzeneacetic Acid; NSC 2753; NSC 27897;
ChemDiv3_014360
3,4-Dimethoxyphenylacetate
bmse000682
UNII-YY50GIT3C7
3,4-Dimethoxybenzeneacetate
3,4-Dimethoxyphenylacetic acid (Homoveratric acid)
(3,4-Dimethoxyphenyl)acetate
SCHEMBL153055
3,4-dimethoxy-phenylacetic acid
3,4-dimethoxyphenyl-acetic acid
DTXCID6048836
NSC2753
HMS1513M16
KUC108679N
3,4-Dimethyloxy phenyl acetic acid
Acetic acid, 3,4-dimethoxyphenyl-
HY-Y0771
NSC27897
s3961
STK299264
3, 4 - Dimethoxy phenyl acetic acid
3,4-Dimethoxyphenylacetic acid, 98%
4,5-Dimethoxy-1,2-benzenacetic Acid
AKOS000119394
BS-4085
CCG-266554
CS-W020108
FD12596
alpha-(3,4-dimethoxyphenyl)acetic acid
IDI1_030158
AC-15716
KSC-11-262-2
SY006121
D0640
EU-0066571
NS00015120
EN300-17388
AK-968/41169417
Homoveratric acid, Vetec(TM) reagent grade, 98%
SR-01000596943
(3,4-Dimethoxyphenyl)acetic Acid(Homoveratric Acid)
SR-01000596943-1
Q10395556
Z56924495
F0902-7631
1000517-77-0
202-244-5