Interesting facts
Interesting Facts about (2-nitrophenyl) N-methylcarbamate
(2-nitrophenyl) N-methylcarbamate is a fascinating compound that demonstrates the intricate relationship between structure and function in organic chemistry. Here are some engaging insights about this intriguing molecule:
- Functional Versatility: This compound features a carbamate functional group, which is known for its ability to act as a versatile intermediate in organic synthesis.
- Biological Relevance: Compounds related to carbamates often showcase bioactivity, making them important in the development of various pharmaceuticals and agrochemicals.
- Nitro Group Influence: The presence of the nitro group on the aromatic ring can significantly affect the reactivity of the compound, often enhancing its electrophilic nature.
- Synthesis Pathways: Understanding the synthesis of (2-nitrophenyl) N-methylcarbamate reveals valuable insights into mechanisms of nucleophilic substitution and electrophilic aromatic substitution reactions.
- Regulatory Significance: As a derivative of carbamate herbicides and pesticides, this compound can be a subject of regulatory scrutiny regarding its environmental impact and safety.
In summary, (2-nitrophenyl) N-methylcarbamate is much more than just a chemical entity; it encapsulates key themes of organic chemistry, including structure-activity relationships and the importance of functional groups in synthesizing biologically active compounds. As mentioned by a leading chemist, "Understanding the nuances of chemical reactivity opens doors to innovations in materials and medicine."
This compound serves as a prime example of how chemistry intertwines with real-world applications.
Synonyms
2-Nitrophenyl N-methylcarbamate
o-Nitrophenyl N-methylcarbamate
7374-06-3
o-Nitrophenyl methylcarbamate
TL-997
Carbamic acid, N-methyl-, 2-nitrophenyl ester
Methylcarbamic ester of 2-nitrophenol
7LQD7G852X
Carbamic acid, methyl-, o-nitrophenyl ester
Carbamic acid, methyl-, 2-nitrophenyl ester
CARBAMIC ACID, N-METHYL-, o-NITROPHENYL ESTER
NSC-128174
(2-nitrophenyl) N-methylcarbamate
AR-2
NSC 128174
BRN 2214975
WLN: WNR BOVM1
UNII-7LQD7G852X
SCHEMBL3640979
CHEMBL3249284
DTXSID70879381
Carbamic acid, o-nitrophenyl ester
Carbamic acid, 2-nitrophenyl ester
NSC128174
N-METHYL-2-NITROPHENYLCARBAMATE
4-06-00-01259 (Beilstein Handbook Reference)
Solubility of (2-nitrophenyl) N-methylcarbamate
(2-nitrophenyl) N-methylcarbamate, with its complex structure, exhibits distinctive solubility characteristics that can be influenced by various factors. Understanding its solubility can provide valuable insights into its behavior in different environments.
Key Points on Solubility:
In summary, while (2-nitrophenyl) N-methylcarbamate is soluble in polar solvents, factors such as temperature, pH, and solvent properties significantly affect its solubility. This compound's behavior in various media should be carefully evaluated for applications in chemical synthesis and formulation.