Interesting facts
Interesting Facts about N-carbamoyl-2-phenyl-acetamide
N-carbamoyl-2-phenyl-acetamide, a fascinating compound, plays a significant role in various fields of chemistry and pharmaceuticals. Here are some intriguing aspects of this compound:
- Chemical Structure: This compound consists of a unique combination of a phenyl ring attached to an acetamide group, which contributes to its biological activity.
- Pharmaceutical Relevance: N-carbamoyl-2-phenyl-acetamide is often studied for its potential therapeutic properties, including anti-inflammatory and analgesic effects.
- Synthesis: Scientists have developed several methods for synthesizing this compound, making it an excellent subject for organic synthesis studies in the laboratory. Techniques may involve urethane transformations or condensation reactions.
- Interdisciplinary Connections: The compound bridges chemistry and medicinal research, illustrating the interplay between small molecules and biological systems.
- Research Potential: Ongoing research aims to explore its derivatives, with scientists investigating modification strategies to enhance efficacy and reduce side effects in pharmaceutical applications.
In conclusion, N-carbamoyl-2-phenyl-acetamide is more than just a chemical entity. Its potential applications in medicine and the intriguing chemistry involved in its synthesis make it a valuable compound worthy of study. As we continue to explore compounds like this, we enhance our understanding of chemical interactions and develop innovative solutions in healthcare.
Synonyms
phenacemide
Phenylacetylurea
Phenurone
63-98-9
Phenacetylurea
Phenuron
Cetylureum
Fenacemid
Neophedan
Phacetur
Phenacalum
Phenacetur
Phenicarb
Phetylureum
Phenacetylcarbamide
Acetylureum
Carbanmide
Comitiadone
Fenacemide
Fenacetamide
Fenostenyl
Neophenal
Phenacereum
Phenarone
Epheron
Epiclase
Felurea
Fenilep
Fenised
Fenural
Fenurea
Fenurone
Fenytan
Phenutal
Phenyrit
Efron
(Phenylacetyl)urea
N-carbamoyl-2-phenylacetamide
Eferon
Phenylacetyluree
Fenacetil-karbamide
Carbamide phenylacetate
Fenylacetylmocovina
Fenacemida
Phenacemidum
Phenacerum
Urea, (phenylacetyl)-
Benzeneacetamide, N-(aminocarbonyl)-
N-(Aminocarbonyl)benzeneacetamide
(2-phenylacetyl)urea
Fenacemida [INN-Spanish]
Phenacemidum [INN-Latin]
A-1348
NSC 39458
HSDB 3380
EINECS 200-570-2
UNII-PAI7J52V09
NSC-39458
BRN 2048735
PAI7J52V09
DTXSID6023442
.alpha.-Phenylacetylurea
Phenacemide [USP:INN:BAN]
CHEBI:8049
DTXCID103442
4-09-00-01636 (Beilstein Handbook Reference)
Fenacemide [DCIT]
NCGC00094754-01
Fenacemida (INN-Spanish)
Phenacemidum (INN-Latin)
PHENACEMIDE (MART.)
PHENACEMIDE [MART.]
Phenylacetyluree [French]
Fenylacetylmocovina [Czech]
Phenacemide (USP:INN:BAN)
CAS-63-98-9
Phenurone (TN)
alpha-Phenylacetylurea
Phenacemide (JAN/INN)
N-(aminocarbonyl)-2-phenylacetamide
N-(Phenylacetyl)urea
Spectrum_000923
N-(Phenylacetyl)urea #
PHENACEMIDE [MI]
Spectrum2_001019
Spectrum3_000679
Spectrum4_000473
Spectrum5_001240
PHENACEMIDE [INN]
PHENACEMIDE [JAN]
WLN: ZVMV1R
PHENACEMIDE [HSDB]
CHEMBL918
PHENACEMIDE [VANDF]
SCHEMBL35118
BSPBio_002377
KBioGR_000946
KBioSS_001403
PHENACEMIDE [WHO-DD]
DivK1c_000320
SPECTRUM1500472
SPBio_001177
GTPL7265
HMS500P22
KBio1_000320
KBio2_001403
KBio2_003971
KBio2_006539
KBio3_001597
PHENACEMIDE [ORANGE BOOK]
NINDS_000320
HMS1920F16
HMS2091N16
Pharmakon1600-01500472
NSC39458
Tox21_111325
CCG-40237
NSC757266
AKOS009156469
Tox21_111325_1
DB01121
NSC-757266
IDI1_000320
NCGC00094754-02
NCGC00094754-03
NCGC00094754-05
SBI-0051478.P003
1ST164431
DB-054589
NS00035612
C07428
D00504
AB00052068_02
EN300-7476381
SR-05000001694
Q3742404
SR-05000001694-1
1-[(C-hydroxycarbonimidoyl)imino]-2-phenylethan-1-ol
BRD-K40905133-001-02-3
BRD-K40905133-001-03-1
BRD-K40905133-001-04-9
200-570-2
Solubility of N-carbamoyl-2-phenyl-acetamide (C9H10N2O2)
N-carbamoyl-2-phenyl-acetamide is a compound that exhibits interesting solubility characteristics. Its solubility can be influenced by several factors, which may include its molecular structure and polarity.
Key Factors Affecting Solubility:
It is essential to consider that while N-carbamoyl-2-phenyl-acetamide may be soluble in water, it could show variable solubility in organic solvents depending on their polarity. This dual behavior allows for various applications in both aqueous and organic environments.
Quotes from Research:
According to studies, "the solubility of amides in water often reflects their potential applications in pharmaceuticals and agrochemicals." This affirms the importance of understanding solubility profiles for practical applications.
In summary, the solubility of N-carbamoyl-2-phenyl-acetamide is determined by its structural features and environmental conditions, making it a versatile compound for various scientific inquiries.