Interesting facts
Interesting Facts about 2-(2-Nitrophenyl)acetonitrile
2-(2-Nitrophenyl)acetonitrile is a fascinating compound that has garnered attention in various fields of chemistry. Here are some interesting aspects to explore:
- Synthetic Applications: This compound serves as an intermediate in the synthesis of numerous pharmaceuticals and agrochemicals, showcasing its importance in organic synthesis.
- Reactivity: The presence of both the nitro and cyano groups in its structure makes 2-(2-nitrophenyl)acetonitrile a versatile reactant. It participates in nucleophilic substitution reactions and can form various derivatives that have valuable chemical properties.
- Research Interest: The compound has been studied for its potential biological activities. Researchers are exploring its antitumor and antimicrobial properties, which could lead to new therapeutic agents.
- Tutorial Importance: In academic settings, this compound often serves as an example in courses covering nucleophilic aromatic substitution and reactivity of aromatic compounds. It allows students to understand complex concepts in practical scenarios.
- Environmental Considerations: Like many nitro compounds, the environmental fate and toxicity of 2-(2-nitrophenyl)acetonitrile are subjects of study, as understanding these attributes is crucial for assessing the safety of chemicals used in agriculture and industry.
As a compound with a rich history of applications and ongoing research, 2-(2-nitrophenyl)acetonitrile illustrates the continuous interplay between organic chemistry and practical applications, revealing just how integral chemistry is to advancements in science and technology.
Synonyms
2-Nitrophenylacetonitrile
610-66-2
(2-Nitrophenyl)acetonitrile
Benzeneacetonitrile, 2-nitro-
(o-Nitrophenyl)acetonitrile
o-Nitrobenzacetonitrile
2-Nitrobenzeneacetonitrile
2-Nitrobenzyl nitrile
Acetonitrile, (o-nitrophenyl)-
o-Nitrophenyl acetonitrile
O-NITROPHENYLACETONITRILE
CCRIS 4681
EINECS 210-231-0
NSC 99338
BRN 1869400
DTXSID7025768
NSC-99338
DTXCID905768
7859F455K6
3-09-00-02283 (Beilstein Handbook Reference)
NITROPHENYL ACETONITRILE, O-
2-NITROPHENYL ACETIC ACID, NITRILE
210-231-0
2-(2-nitrophenyl)acetonitrile
2-Nitrobenzyl Cyanide
2-Nitrobenzylcyanide
MFCD00007183
(2-nitrophenyl)-acetonitrile
o-nitrobenzyl cyanide
(2-Nitro-phenyl)-acetonitrile
UNII-7859F455K6
NSC99338
2-Nitro-benzyl-cyanid
NCIOpen2_002167
SCHEMBL181041
2-(2-nitrophenyl)-acetonitrile
2-Nitrophenylacetonitrile, 98%
CHEMBL1300441
BCP32231
Tox21_200975
AKOS000122139
CS-W002025
FN26291
GS-3235
NCGC00090864-01
NCGC00090864-02
NCGC00258528-01
CAS-610-66-2
SY006137
DB-005254
N0781
NS00034550
EN300-01351
2-Nitrobenzyl Cyanide;O-nitrophenylacetonitrile
Q27266640
Z56886385
InChI=1/C8H6N2O2/c9-6-5-7-3-1-2-4-8(7)10(11)12/h1-4H,5H
Solubility of 2-(2-nitrophenyl)acetonitrile
2-(2-nitrophenyl)acetonitrile, with the chemical formula C9H8N2O2, exhibits intriguing solubility characteristics that are influenced by its molecular structure and functional groups.
When considering its solubility, it is essential to recognize the following points:
In summary, this compound's solubility is promoted by its polar functional groups, making it more soluble in polar solvents compared to non-polar environments. It is crucial to always consult solubility tables or conduct empirical tests to ascertain the exact solubility conditions.