Interesting facts
Interesting Facts About Methyl 4-Acetamido-2-Ethoxy-Benzoate
Methyl 4-acetamido-2-ethoxy-benzoate, often referred to in the chemical literature, is a compound that showcases a variety of interesting properties and applications:
- Structural Insights: The presence of both an ethoxy group and an acetamido group in its structure contributes to its unique reactivity and solubility characteristics, making it a significant compound in organic chemistry.
- Biological Relevance: This compound has garnered attention for its potential use in medicinal chemistry. Compounds with similar structures are often investigated for their anti-inflammatory and analgesic properties.
- Synthesis Pathways: The synthesis of this compound often involves various organic reactions, including Esterification and Acetylation, illustrating fundamental concepts in organic synthesis.
- Applications in Research: Methyl 4-acetamido-2-ethoxy-benzoate serves as an important intermediate in the synthesis of more complex molecules. Its derivatives may even lead to the discovery of new pharmaceuticals.
- Chemical Behavior: The compound’s reactivity can be influenced by the substituents on the aromatic ring, leading to interesting studies in substitution reactions and mechanistic chemistry.
As with many compounds in organic chemistry, understanding methyl 4-acetamido-2-ethoxy-benzoate opens the door to a greater appreciation for the complexity and interconnectedness of chemical systems. Each component of the molecule plays a role in determining its properties, reactions, and ultimately, its applications in various scientific fields.
Synonyms
ETHOPABATE
Methyl 4-acetamido-2-ethoxybenzoate
59-06-3
Ethopabat
Benzoic acid, 4-(acetylamino)-2-ethoxy-, methyl ester
EINECS 200-414-3
MFCD00075809
UNII-F4X3L6068O
Methyl 4-(acetylamino)-2-ethoxybenzoate
DTXSID6046264
4-Acetamido-2-ethoxybenzoesaeuremethylester
F4X3L6068O
Ethopabate [USP:BAN]
DTXCID4026264
NCGC00160624-01
Ethopabate 100 microg/mL in Acetonitrile
Ethopabate (USP:BAN)
Ethyl Pabate
ETHOPABATE (MART.)
ETHOPABATE [MART.]
ETHOPABATE (USP-RS)
ETHOPABATE [USP-RS]
ETHOPABATE (USP MONOGRAPH)
ETHOPABATE [USP MONOGRAPH]
CAS-59-06-3
Amprol Plus (veterinary)
Methyl4-acetamido-2-ethoxybenzoate
Ethopabate (USP)
Methyl 2-ethoxy-4-acetamidobenzoate
Ethopabate (Standard)
Ethopabate - Technical
ETHOPABATE [MI]
4-acetylamino-2-ethoxybenzoic acid methyl ester
SCHEMBL540932
CHEMBL458769
ETHOPABATE [GREEN BOOK]
HY-B2138R
CHEBI:183844
HY-B2138
Tox21 111943
Tox21_111943
s3707
Methyl 4-acetamido-2-ethoxy-benzoate
AKOS015892662
Tox21_111943_1
CCG-213430
CS-8028
FE22866
NCGC00160624-02
NCGC00160624-03
NCGC00160624-04
AS-11898
SY226309
DB-053312
NS00000013
4-Acetamido-2-ethoxybenzoic acid, methyl ester
D08916
Ethopabate, VETRANAL(TM), analytical standard
AB01563313_01
4-Acetylamino-2-ethoxy-benzoic acid, methyl ester
SR-01000944203
Q5404419
SR-01000944203-1
BRD-K02475039-001-01-0
Ethopabate, British Pharmacopoeia (BP) Reference Standard
Ethopabate, United States Pharmacopeia (USP) Reference Standard
200-414-3
4-Acetylamino-2-ethoxy-benzoic acid methyl ester;4-acetamido-2-ethoxy-benzoic acid methyl ester;4-Acetamido-2-ethoxybenzoic acid met hyl ester
Solubility of Methyl 4-Acetamido-2-ethoxy-benzoate (C12H15NO4)
Methyl 4-acetamido-2-ethoxy-benzoate is a compound that exhibits intriguing solubility characteristics. Generally, the solubility of this ester can be influenced by various factors, including polarity, molecular structure, and the presence of functional groups.
Factors Influencing Solubility
In conclusion, methyl 4-acetamido-2-ethoxy-benzoate exhibits a moderate solubility profile, showcasing a versatile behavior in different solvent environments. Understanding its solubility can be crucial for applications in pharmaceuticals and chemical synthesis.