Interesting facts
Interesting Facts About 2-[(4-chlorobenzoyl)amino]acetic acid
2-[(4-chlorobenzoyl)amino]acetic acid is a fascinating compound that belongs to the class of amino acids and synthetic pharmaceuticals. Below are some intriguing aspects that highlight its significance in the field of chemistry and pharmacology:
- Dual Functionality: This compound serves as both an amino acid due to the presence of the amino group and as a carboxylic acid, indicating its potential use in various biological systems.
- Chlorobenzoyl Substitution: The presence of the 4-chlorobenzoyl group enhances its lipophilicity, allowing this compound to interact effectively with biological membranes.
- Medicinal Applications: It has garnered attention for its potential role in designing therapeutic agents, particularly in anti-inflammatory and analgesic drugs.
- Research Insights: Studies have shown that compounds with similar structures can exhibit a range of pharmacological activities, from acting as enzyme inhibitors to modulating receptor functions.
- Environmental Considerations: The chlorine atom in the structure may impact the compound's environmental behavior, raising questions about its persistence and potential effects on ecosystems.
Considering the ongoing research and development in medicinal chemistry, 2-[(4-chlorobenzoyl)amino]acetic acid stands out as a compound with significant potential.
As the field continues to evolve, understanding such compounds could pave the way for innovative treatments and therapeutic solutions.
Synonyms
13450-77-6
4-Chlorohippuric acid
p-Chlorohippuric acid
Glycine, N-(4-chlorobenzoyl)-
p-Chlorobenzoylglycine
4-Chlorobenzoylglycine
N-(p-Chlorobenzoyl)glycine
HIPPURIC ACID, p-CHLORO-
N-(4-Chlorobenzoyl)glycine
92HJ692NVA
DTXSID40158756
DTXCID7081247
2-(4-Chlorobenzamido)acetic acid
2-[(4-chlorobenzoyl)amino]acetic acid
(4-Chloro-benzoylamino)-acetic acid
MFCD00020447
2-[(4-chlorophenyl)formamido]acetic acid
CHEMBL462
2-[(4-chlorophenyl)carbonylamino]acetic acid
[(4-chlorophenyl)formamido]acetic acid
BRN 1110511
UNII-92HJ692NVA
AI3-30805
Glycine,N-(4-chlorobenzoyl)-
2-(4-Chlorobenzamido)aceticacid
4-Chlorobenzoylglycine; N-(4-Chlorobenzoyl)glycine; N-(p-Chlorobenzoyl)glycine; Ro 11-1903; p-Chlorobenzoylglycine; p-Chlorohippuric Acid
Moclobemide metabolite M9
Cambridge id 5190259
Oprea1_302425
Oprea1_822134
3-09-00-01364 (Beilstein Handbook Reference)
SCHEMBL4002486
COYZIYOEXGRBHQ-UHFFFAOYSA-N
ALBB-033219
NAA45077
BDBM50016616
N-[(4-chlorophenyl)carbonyl]glycine
SBB004563
STK036747
AKOS000114598
PITOLISANT METABOLITE BP1.10556
ST055065
BP1.10556
CS-0157556
EN300-00184
3E-929
C72366
SR-01000412838
SR-01000412838-1
Q27271504
Z56840113
F0345-3965
Solubility of 2-[(4-chlorobenzoyl)amino]acetic acid
The solubility of 2-[(4-chlorobenzoyl)amino]acetic acid, also known as a derivative of amino acids, is influenced by several key factors. Understanding its solubility can provide insights into its behavior in various environments:
In practical applications, it is quoted that "solubility is a gateway to chemical reactivity." Therefore, comprehending how 2-[(4-chlorobenzoyl)amino]acetic acid interacts with solvents aids in its utilization in pharmaceuticals and other industries.
In summary, while this compound exhibits promising solubility characteristics, further studies may be needed to elucidate the precise solubility parameters under varying conditions.