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2-(4-Nitrophenoxy)acetic acid

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Identification
Molecular formula
C8H7NO5
CAS number
31662-55-0
IUPAC name
2-(4-nitrophenoxy)acetic acid
State
State

At room temperature, 2-(4-Nitrophenoxy)acetic acid is a solid. It forms crystalline structures and is typically handled in its solid state for reactions and applications.

Melting point (Celsius)
174.00
Melting point (Kelvin)
447.15
Boiling point (Celsius)
344.50
Boiling point (Kelvin)
617.65
General information
Molecular weight
195.15g/mol
Molar mass
195.1480g/mol
Density
1.4740g/cm3
Appearence

2-(4-Nitrophenoxy)acetic acid appears as a pale yellow crystalline solid. It is often found in its powder form. The solid is slightly soluble in water and can form brilliant yellow to orange solutions when dissolved in organic solvents.

Comment on solubility

Solubility of 2-(4-nitrophenoxy)acetic acid

2-(4-Nitrophenoxy)acetic acid is a fascinating compound when it comes to its solubility characteristics. This compound, with the chemical formula C9H9NO4, exhibits a unique interaction with solvents due to the presence of both the nitro group and the carboxylic acid functional group. Here's what you need to know about its solubility:

  • Polarity: The presence of the polar carboxylic acid group enhances its solubility in polar solvents.
  • Solvent Compatibility: It is typically soluble in water and alcohols, as these solvents can engage in hydrogen bonding with the carboxylic acid group.
  • Hydrophobic Regions: The aromatic nitro group can also play a role in solubility. While it adds some hydrophobic character, the overall polarity remains significant.

In summary, 2-(4-nitrophenoxy)acetic acid is likely to be more soluble in polar solvents compared to non-polar ones. Its solubility enhances its utility in various chemical applications, especially in organic synthesis and pharmaceuticals.

Interesting facts

Interesting Facts about 2-(4-Nitrophenoxy)acetic Acid

2-(4-Nitrophenoxy)acetic acid is a fascinating compound that combines the attributes of both a carboxylic acid and an aromatic ether. This unique structure contributes to its diverse applications in various fields, particularly in agricultural chemistry and pharmaceutical research.

Applications of 2-(4-Nitrophenoxy)acetic Acid

  • Herbicidal Properties: This compound is known for its effectiveness as a herbicide, where it acts to inhibit the growth of unwanted plants.
  • Biological Research: Researchers study its effects on plant growth and development, making it a key compound in agrochemical studies.
  • Pharmaceutical Intermediates: Its role as a precursor in the synthesis of various drugs highlights its utility in medicinal chemistry.

Key Characteristics

One of the intriguing aspects of 2-(4-nitrophenoxy)acetic acid is its electron-withdrawing nitro group, which significantly affects its chemical reactivity and biological activity. This property can alter metabolic pathways in organisms, leading researchers to explore its use in targeting specific sites within biological systems.

As with many compounds in the realm of organic chemistry, the research surrounding 2-(4-nitrophenoxy)acetic acid can lead to discoveries of new chemical properties, expanding its applicability in agriculture and medicine. Its substantial influence in these areas underscores the importance of understanding the nuanced chemistry behind such compounds.

Did You Know?

Many researchers refer to 2-(4-nitrophenoxy)acetic acid as a "versatile building block" in organic chemistry, capable of leading to a myriad of derivatives with varying biological activities. This versatility is particularly valuable as it allows chemists to tailor compounds for specific functions, maximizing their efficiency in real-world applications.

In conclusion, 2-(4-nitrophenoxy)acetic acid is not just another chemical compound; it represents the intersection of science and application, showcasing how molecules can have profound impacts on both the environment and human health.

Synonyms
4-Nitrophenoxyacetic acid
(4-Nitrophenoxy)acetic acid
p-Nitrophenoxyacetic acid
Acetic acid, 2-(4-nitrophenoxy)-
Acetic acid, (4-nitrophenoxy)-
Ba 2690
ACETIC ACID, p-NITROPHENOXY-
EINECS 217-283-3
NSC 166278
BRN 2051970
AI3-52610
DTXSID3061978
4-06-00-01302 (Beilstein Handbook Reference)
DTXCID8035710
217-283-3
avdlfionkhgqap-uhfffaoysa-n
1798-11-4
2-(4-Nitrophenoxy)acetic acid
(4-Nitro-phenoxy)-acetic acid
2-(4-Nitrophenoxy)aceticacid
2-(4-Nitrophenoxy)-acetic acid
2-(4-Nitrophenoxy)acetic Acid; (4-Nitrophenoxy)acetic Acid; (p-Nitrophenoxy)acetic Acid; Ba 2690; NSC 166278; alpha-(4-Nitrophenoxy)acetic Acid
MFCD00017030
4-nitrophenoxy acetic acid
Oprea1_291146
(4-nitrophenoxy) acetic acid
(4-nitrophenoxy)-acetic acid
SCHEMBL656493
(4-Nitro phenoxy)acetic Acid
(4-Nitro phenoxy) acetic acid
CHEMBL177045
Acetic acid, (p-nitrophenoxy)-
2-(4-nitro-phenoxy)-acetic acid
ALBB-000229
BBL023111
NSC166278
STK093391
AKOS000264482
CS-W015679
FN55024
NSC-166278
AS-60943
N0226
NS00025921
EN300-10631
E85242
AF-615/00098055
SR-01000409228
SR-01000409228-1
Z56347386
(4-nitrophenoxy)acetic acid - 2,2',2''-nitrilotriethanol (1:1)