Interesting facts
Interesting Facts about N-carbamoyl-2-isopropyl-pent-4-enamide
N-carbamoyl-2-isopropyl-pent-4-enamide is a fascinating compound with a unique structure that gives it special properties and potential applications. Here are some intriguing insights:
- Structural Complexity: This compound features a carbamoyl group which is well-known for its role in biological systems, particularly in amino acid metabolism. Its presence enhances the compound's reactivity.
- Versatility: Due to its pent-4-enamide framework, N-carbamoyl-2-isopropyl-pent-4-enamide can potentially act as a versatile building block for the synthesis of more complex molecules.
- Biological Relevance: Compounds like N-carbamoyl-2-isopropyl-pent-4-enamide are often studied in the context of drug development because of their ability to interact with biological targets.
- Potential Applications: Given its structure, this compound could find applications in agrochemicals, pharmaceuticals, and even materials science.
- Research Opportunities: The study of this compound provides an exciting opportunity for chemists to explore its reactivity, mechanism of action, and potential therapeutic uses.
In conclusion, N-carbamoyl-2-isopropyl-pent-4-enamide embodies the intersection of organic chemistry and medicinal research, making it a compound worth studying for its possible implications in numerous scientific fields.
Synonyms
Apronal
Allylisopropylacetylurea
APRONALIDE
528-92-7
Isodormid
Sedormid
(2-Isopropyl-4-pentenoyl)urea
Allylisopropylacetylcarbamide
(2-Isopropylpent-4-enoyl)urea
Isopropylallylazetylkarbamid
Urea, (2-isopropyl-4-pentenoyl)-
N-(Aminocarbonyl)-2-(1-methylethyl)-4-pentenamide
EINECS 208-443-3
Isopropylallylazetylkarbamid [German]
BRN 1775529
V18J24E25E
APRONALIDE [MI]
APRONAL [WHO-DD]
[2-(propan-2-yl)pent-4-enoyl]urea
4-Pentenamide, N-(aminocarbonyl)-2-(1-methylethyl)-
DTXSID00862125
(2-(propan-2-yl)pent-4-enoyl)urea
DTXCID10810935
(+-)-apronalide
apronalide, (+-)-
ALLYL ISOPROPYL ACETYLUREA
N-carbamoyl-2-propan-2-ylpent-4-enamide
(+/-)-APRONALIDE
APRONALIDE, (+/-)-
Allylisopropylacetylurea;Apronalide
UNII-V18J24E25E
MFCD00210239
Allylisoprorylacetylurea
(Allylisopropylacetyl)urea
SCHEMBL662209
(Allylisopropylacetyl)carbamide
CHEMBL509282
KSUUMAWCGDNLFK-UHFFFAOYSA-
CHEBI:134827
N-(2-Isopropyl-4-pentenoyl)urea
2-Isopropyl-4-pentenoyl-harnstoff
Apronalide 1.0 mg/ml in Methanol
HY-B2177
N-(2-Isopropyl-4-pentenoyl)urea #
s6450
AKOS006272745
N-Carbamoyl-2-isopropyl-4-pentenamide
CS-7723
DB13221
AS-58738
DB-361963
A2844
N-(aminocarbonyl)-2-isopropylpent-4-enamide
NS00042922
D03975
D88535
EN300-8092389
Q1095009
InChI=1/C9H16N2O2/c1-4-5-7(6(2)3)8(12)11-9(10)13/h4,6-7H,1,5H2,2-3H3,(H3,10,11,12,13)
Solubility of N-carbamoyl-2-isopropyl-pent-4-enamide
The solubility of N-carbamoyl-2-isopropyl-pent-4-enamide is influenced by its molecular structure, including functional groups and the overall polarity of the compound. Characteristics affecting solubility include:
In general, one might expect N-carbamoyl-2-isopropyl-pent-4-enamide to demonstrate:
It is crucial to conduct empirical experiments to determine exact solubility parameters, as theoretical predictions can vary based on specific conditions. Understanding the solubility of this compound aids in its applications and interactions within various chemical environments.