Skip to main content

Phenylsuccinic acid

ADVERTISEMENT
Identification
Molecular formula
C10H10O4
CAS number
635-51-8
IUPAC name
2-benzylbutanedioic acid
State
State
Phenylsuccinic acid is a solid at room temperature.
Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
552.00
Boiling point (Kelvin)
825.15
General information
Molecular weight
194.19g/mol
Molar mass
194.1920g/mol
Density
1.2846g/cm3
Appearence

Phenylsuccinic acid appears as white crystalline powder.

Comment on solubility

Solubility of 2-benzylbutanedioic acid (C10H10O4)

2-benzylbutanedioic acid, a unique di-carboxylic acid, exhibits interesting solubility characteristics that are influenced by its molecular structure. The solubility of this compound can be summarized as follows:

  • Water Solubility: Generally, 2-benzylbutanedioic acid is expected to have limited solubility in water due to the presence of its hydrophobic benzyl group, which can hinder interactions with polar water molecules.
  • Solvent Compatibility: This compound tends to be more soluble in organic solvents such as ethanol, methanol, and dichloromethane, where its nonpolar characteristics enhance solubility.
  • Influence of Temperature: As with many organic compounds, solubility can increase with temperature. Heating the solvent may improve the dissolution of 2-benzylbutanedioic acid in organic media.

In conclusion, while 2-benzylbutanedioic acid is not highly soluble in water, its solubility profile in organic solvents makes it a versatile compound for various applications. Understanding the solubility behavior is essential for effectively utilizing this compound in chemical processes.

Interesting facts

Interesting Facts about 2-benzylbutanedioic acid

2-benzylbutanedioic acid, often referred to in scientific contexts by its IUPAC name, is a fascinating compound in the realm of organic chemistry. As a dicarboxylic acid, it contains two acidic functional groups, which play a crucial role in its chemical behavior and reactivity. Here are some compelling highlights:

  • Structure and Functionality: The presence of both carboxylic acid groups greatly expands the compound's ability to interact with various biological and chemical systems. This dual functionality can lead to interesting applications in medicinal chemistry.
  • Biological Relevance: Compounds similar to 2-benzylbutanedioic acid may exhibit biological activity, making them potential candidates for drug development or as biochemical probes in research.
  • Synthesis Pathways: The synthesis of 2-benzylbutanedioic acid is notable for its straightforward synthetic routes, often involving condensation reactions that are essential in organic synthesis. This makes it a favored choice in academic and industrial laboratories.
  • Research Applications: Due to its intriguing chemical properties, 2-benzylbutanedioic acid is often explored for its potential role as an intermediate in organic reactions and material science.
  • Versatile Derivatives: By altering its structure, a wide variety of derivatives can be created, each with unique properties and potential applications, highlighting the importance of structural modification in organic chemistry.

In conclusion, 2-benzylbutanedioic acid is not just a simple compound—its rich chemistry and potential applications make it a subject of significant interest in both academic and applied chemistry fields. As the saying goes in chemistry, *"The excitement lies in the functional diversity of organic compounds."* By exploring these compounds, scientists can unlock new possibilities in both research and industry.

Synonyms
2-Benzylsuccinic acid
884-33-3
DL-Benzylsuccinic acid
2-benzylbutanedioic acid
Benzylsuccinic acid
36092-42-9
D,L-Benzylsuccinic Acid
alpha-Benzylsuccinic acid
MFCD00055798
NSC20708
NSC 20708
.alpha.-Benzylsuccinic acid
(phenylmethyl)butanedioic acid
beta-carboxybenzenebutanoic acid
CHEMBL151284
CHEBI:16054
DTXSID90859847
Butanedioic acid, (phenylmethyl)-
Benzenebutanoic acid, .beta.-carboxy-
NSC-20708
(2R)-2-(Phenylmethyl)butanedioic acid
2-Benzyl-succinic acid
mono benzyl succinic acid
2-Benzylsuccinic acid #
alpha -Benzylsuccinic acid
CBMicro_015697
Mitiglinide intermediate 2
Oprea1_299272
SCHEMBL393002
DL-Benzylsuccinic acid, >=99%
DTXCID10210395
HMS1608A16
BCP12215
BBL028067
BDBM50121929
s6123
STK524740
AKOS001600536
AKOS016038118
CCG-103996
FB18545
HY-W044764
SB46650
NCGC00322037-01
AS-10262
NCI60_001739
SY003042
SY040253
BIM-0015709.P001
DB-020567
CS-0037767
Butanedioic acid, (phenylmethyl)-, (+/-)-
Butanedioic acid, (phenylmethyl)-, (A+/-)-
EN300-109182
AB01317455-02
Q27098354
Z1418939706
2-(Phenylmethyl)butanedioic acid;Benzylsuccinic acid;NSC 20708
677-214-1
688-412-2