Interesting facts
Intriguing Insights into N-(o-tolyl)-3-oxo-butanamide
N-(o-tolyl)-3-oxo-butanamide is an organic compound that has drawn attention for its intriguing structure and potential applications. As a member of the amide functional group, it showcases a fascinating blend of characteristics that are valued in both synthetic chemistry and various industries. Here are some interesting facts about this compound:
- Structural Diversity: The compound features a unique blend of a keto group and an amide linkage, which allows for a variety of chemical reactions and transformations, making it a versatile building block in organic synthesis.
- Biological Significance: Compounds of this class often exhibit interesting biological properties, including anti-inflammatory and analgesic activities, making them a subject of biological research.
- Common Derivative: The presence of an o-tolyl group in its structure suggests it may be related to other substituted aromatic compounds, raising questions about its role in medicinal chemistry and its potential as a therapeutic agent.
- Synthetic Utility: This compound can be synthesized through various methods, including acylation reactions. Chemists appreciate such compounds for their potential use in the development of new materials and pharmaceuticals.
- Application in Industry: Beyond research, derivatives of amides are commonly utilized in agrochemicals, plastics, and as intermediates in the synthesis of numerous compounds, underscoring their industrial relevance.
In summary, N-(o-tolyl)-3-oxo-butanamide is more than just a chemical compound; it serves as a valuable tool in the chemistry toolkit. Its reactivity, structural complexity, and potential applications in medicinal and industrial chemistry make it a fascinating subject for both chemists and engineers alike.
Synonyms
2'-Methylacetoacetanilide
93-68-5
N-(2-Methylphenyl)-3-oxobutanamide
N-Acetoacetyl-o-toluidine
O-Acetoacetotoluidide
Acetoacet-o-toluidide
2-Acetoacetylaminotoluene
Acetoacet-o-toluidine
3-Oxo-N-(o-tolyl)butanamide
Butanamide, N-(2-methylphenyl)-3-oxo-
2-Acetoacetotoluidide
Acetoacetyl-2-methylanilide
2'-Methylacetoacetanilide (AAOT)
Acetoaceto-ortho-toluidide
NSC 7655
CCRIS 7750
Acetoacet-ortho-toluidide
UNII-MCN1GV8J3R
MCN1GV8J3R
EINECS 202-267-0
BRN 2099098
DTXSID3026562
AI3-08708
ortho-Acetoacetotoluidide
NSC-7655
MFCD00008782
DTXCID206562
EC 202-267-0
4-12-00-01777 (Beilstein Handbook Reference)
CAS-93-68-5
AAOT
NSC7655
2\'-Methylacetoacetanilide
WLN: 1V1VMR B
o-Acetoacetotoluidide, 98%
N-Acetoacetyl-2-methylaniline
SCHEMBL382223
CHEMBL1893178
Tox21_201308
Tox21_303146
STK400317
AKOS000120625
BS-4052
N-(2-Methylphenyl)-3-oxobutanamide #
NCGC00164200-01
NCGC00164200-02
NCGC00256990-01
NCGC00258860-01
DB-057420
A1020
NS00005760
EN300-18263
N~1~-(2-METHYLPHENYL)-3-OXOBUTANAMIDE
Q27283887
Z57708665
F1723-0105
202-267-0
Solubility of N-(o-tolyl)-3-oxo-butanamide
N-(o-tolyl)-3-oxo-butanamide is an intriguing compound with specific solubility characteristics that can influence its applications and behavior in various environments. Understanding the solubility of this compound is crucial for its effective use in chemical reactions and formulations.
In general, the solubility of organic compounds like N-(o-tolyl)-3-oxo-butanamide can be affected by multiple factors such as:
Specifically for N-(o-tolyl)-3-oxo-butanamide, it might be more soluble in:
However, it is expected to have limited solubility in water because of the hydrophobicity contributed by the o-tolyl group. This characteristic can limit its use in aqueous environments.
In conclusion, while N-(o-tolyl)-3-oxo-butanamide demonstrates interesting solubility behavior, it is essential to conduct specific experimental investigations to determine its solubility in various solvents under different conditions.