Interesting facts
Interesting Facts about (4-nitrophenyl) 2-(benzyloxycarbonylamino)acetate
(4-nitrophenyl) 2-(benzyloxycarbonylamino)acetate is a fascinating compound that lies at the intersection of organic chemistry and medicinal applications. This compound, often referred to in synthetic organic chemistry, has garnered attention for several reasons:
- Structure and Functionality: This compound features a distinctive 4-nitrophenyl group, lending it unique reactivity and properties. The presence of the benzyloxycarbonylamino moiety enhances its potential for applications in pharmaceuticals.
- Versatile Intermediate: It serves as a versatile intermediate in various organic syntheses. Its ability to undergo further reactions makes it valuable in the synthesis of more complex molecules.
- Biological Significance: The compound is often studied for its role in drug development, particularly in the creation of enzyme inhibitors. Its structural features can mimic natural substrates, making it useful for understanding enzyme mechanisms.
- Application in Research: In the field of medicinal chemistry, it can be used as a starting material for synthesizing compounds with antibacterial or anticancer properties, illustrating its potential impact on health and disease treatment.
- Analytical Utility: Due to its distinctive characteristics, (4-nitrophenyl) 2-(benzyloxycarbonylamino)acetate can serve as a probe in various analytical techniques, aiding scientists in the elucidation of reaction pathways.
As the complexity of organic synthesis continues to evolve, compounds like (4-nitrophenyl) 2-(benzyloxycarbonylamino)acetate demonstrate the intricate relationship between structure and reactivity. Researchers often emphasize that "understanding these compounds is key to unlocking new frontiers in drug design and development." With ongoing studies, the potential applications of this compound could lead to significant advancements in therapeutic strategies.
Synonyms
4-Nitrophenyl N-((phenylmethoxy)carbonyl)glycinate
4-nitrophenyl N-[(phenylmethoxy)carbonyl]glycinate
217-097-2
Z-Gly-ONp
1738-86-9
N-Carbobenzoxyglycine 4-Nitrophenyl Ester
Z-glycine 4-nitrophenyl ester
4-Nitrophenyl ((benzyloxy)carbonyl)glycinate
(4-nitrophenyl) 2-(phenylmethoxycarbonylamino)acetate
N-Benzyloxycarbonylglycine 4-nitrophenyl ester
N-Carbobenzoxyglycine p-nitrophenyl ester
Carbobenzyloxyglycine 4-nitrophenyl ester
Glycine, N-((phenylmethoxy)carbonyl)-, 4-nitrophenyl ester
GLYCINE, N-CARBOXY-, N-BENZYL ESTER, p-NITROPHENYL ESTER
Glycine, N-[(phenylmethoxy)carbonyl]-, 4-nitrophenyl ester
N-Cbz-glycine 4-Nitrophenyl Ester
EINECS 217-097-2
NSC 405051
BRN 1916980
p-Nitrophenylcarbobenzoxyglycine
N-Cbz-glycine p-nitrophenyl ester
Z-Gly-Nph
MFCD00024663
N-Cbz-Gly-ONp
benzyloxycarbonyl-glycine p-nitrophenyl ester
CHEMBL12788
4-nitrophenyl 2-{[(benzyloxy)carbonyl]amino}acetate
4-Nitrophenyl 2-(((benzyloxy)-carbonyl)amino)acetate
SCHEMBL1803004
DTXSID30169659
NSC405051
AKOS016003463
Carbobenzoxyglycine p-nitrophenyl ester
HY-W111209
NSC-405051
AS-49143
CS-0169318
NS00025708
n-benzyloxycarbonyl glycine p-nitrophenyl ester
N-benzyloxycarbonylglycine para-nitrophenyl ester
4-Nitrophenyl ([(benzyloxy)carbonyl]amino)acetate #
N- alpha -Benzyloxycarbonyl-Gly p-nitrophenyl ester
N-CarbobenZoxyglycine-4-nitrophenyl ester (CbZ-Gly-ONp)
Solubility of (4-nitrophenyl) 2-(benzyloxycarbonylamino)acetate
The solubility of (4-nitrophenyl) 2-(benzyloxycarbonylamino)acetate is an intriguing topic due to its complex molecular structure. Understanding its solubility characteristics is crucial for potential applications in various fields.
Here are several key points regarding its solubility:
In summary, the solubility of (4-nitrophenyl) 2-(benzyloxycarbonylamino)acetate can be influenced by a variety of factors including solvent type, temperature, and pH conditions. The nuanced behavior of this compound in solution is a fascinating area of study, highlighting the intricate relationships between molecular structure and solubility.