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4-anilino-4-oxo-butanoic acid

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Identification
Molecular formula
C10H11NO3
CAS number
89284-92-6
IUPAC name
4-anilino-4-oxo-butanoic acid
State
State

At room temperature, 4-anilino-4-oxo-butanoic acid is in a solid state. Due to its high melting point, it remains stable as a solid under standard conditions.

Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
580.00
Boiling point (Kelvin)
853.15
General information
Molecular weight
193.21g/mol
Molar mass
193.2090g/mol
Density
1.2345g/cm3
Appearence

4-Anilino-4-oxo-butanoic acid appears as a crystalline solid. It is pale yellow to beige in color. This compound might exhibit a slightly aromatic odor due to the presence of the anilino group.

Comment on solubility

Solubility of 4-anilino-4-oxo-butanoic acid

4-anilino-4-oxo-butanoic acid, with its intriguing molecular structure, presents notable properties regarding solubility. The solubility of this compound can be influenced by various factors including temperature, pH, and the presence of solvents. Here are some key points to consider:

  • Polarity: The presence of polar functional groups enhances its ability to dissolve in polar solvents, such as water.
  • pH Dependence: The acid nature of this compound means its solubility may increase in alkaline solutions where deprotonation occurs.
  • Temperature Effects: Increasing the temperature often elevates solubility due to enhanced molecular motion, which can disrupt intermolecular forces.

In summary, the solubility of 4-anilino-4-oxo-butanoic acid is characterized by its responsiveness to environmental conditions. It's important to experiment with different solvents and temperature ranges to find optimal conditions for dissolution. As the phrase goes, 'dissolution is often a balancing act of forces.'

Interesting facts

Facts About 4-Anilino-4-oxo-butanoic Acid

4-Anilino-4-oxo-butanoic acid is an intriguing compound that showcases fascinating properties and applications within the realm of organic chemistry. Often noted for its role in the development of pharmaceuticals, this compound is of significant interest due to its structural features and potential benefits.

Chemical Structure and Characteristics

The unique structure of 4-anilino-4-oxo-butanoic acid includes:

  • Aniline moiety: This functional group often imparts various biological activities to the compound.
  • Carbonyl group: The presence of the carbonyl group is crucial for its reactivity, allowing for condensation and further chemical transformations.
  • Acidic functionality: As a carboxylic acid, it contributes to the compound's ability to participate in acid-base reactions.

Applications and Significance

This compound is predominantly studied for its impact in various fields:

  • Pharmaceutical Chemistry: 4-anilino-4-oxo-butanoic acid is often investigated for its potential as a lead compound in drug design.
  • Biological Studies: Its aniline component can lead to the exploration of numerous biological pathways and mechanisms.
  • Synthetic Reactions: It serves as a versatile building block for synthesizing more complex molecules.

Interesting Insights

Anilines, in general, have been a focal point in chemical research due to their remarkable ability to:

  • Act as both a nucleophile and electrophile in various reactions, allowing for versatile synthetic routes.
  • Undergo azo coupling reactions, which are crucial in dye chemistry and material science.

In essence, 4-anilino-4-oxo-butanoic acid is more than just a chemical compound; it represents the intersection of chemistry and biology, paving the way for innovations in drug development and material science. Its engaging structural characteristics and application potential make it a subject worthy of detailed exploration among chemists and students alike.

Synonyms
4-Anilino-4-oxobutanoic acid
102-14-7
Succinanilic acid
4-Oxo-4-(phenylamino)butanoic acid
N-Phenylsuccinamic acid
Succinic monoanilide
Succinic acid monoanilide
4-Oxo-4-phenylaminobutanoic acid
BUTANOIC ACID, 4-OXO-4-(PHENYLAMINO)-
N-Phenylbutanedioic acid monoamide
N-Phenyl-succinamic acid
MFCD00029825
NSC 56471
UNII-L4V0G8222E
BRN 2806264
L4V0G8222E
NSC-56471
Succinamic acid, N-phenyl-
SUCCINANILIC ACID [MI]
CHEMBL152730
DTXSID20144511
4-12-00-00468 (Beilstein Handbook Reference)
NSC56471
Propionic acid, 3-(phenylcarbamoyl)-
L-000341257
3-(phenylcarbamoyl)propanoic acid
Succinanilsaure
Butanoic acid,4-oxo-4-(phenylamino)-
Maybridge1_006842
ChemDiv2_000397
Cambridge id 5133967
Oprea1_388074
Oprea1_552059
SCHEMBL94252
4-anilino-4-oxo-butanoic acid
DTXCID0067002
HMS560O22
CHEBI:173931
KTFGFGGLCMGYTP-UHFFFAOYSA-N
HMS1370C01
4-Oxo-4-(phenylamino)butanoicacid
ALBB-012006
BBL036006
BDBM50136839
CCG-44906
STK018310
AKOS000296139
CS-W010689
FA17935
AS-32051
SR-01000418000
SR-01000418000-1
SR-01000418000-2
Q27282710
Z56176896
F0722-4214
N-Phenyl-succinamic acid;Butanedioic acid anilide;4-Oxo-4-(phenylamino)butanoic acid